SitesBLAST
Comparing WP_007691434.1 NCBI__GCF_000336675.1:WP_007691434.1 to proteins with known functional sites using BLASTp with E ≤ 0.001.
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Found 13 hits to proteins with known functional sites (download)
4xfjB Crystal structure of argininosuccinate synthase from mycobacterium thermoresistibile in complex with amppnp and arginine
40% identity, 92% coverage: 10:398/425 of query aligns to 1:393/397 of 4xfjB
- active site: D13 (= D22), R94 (= R101), D123 (= D130), S174 (= S179)
- binding phosphoaminophosphonic acid-adenylate ester: A7 (= A16), Y8 (≠ F17), S9 (= S18), T14 (= T23), I34 (≠ V44), G116 (= G123), C117 (= C124), F127 (= F134)
- binding arginine: Y86 (= Y93), S90 (≠ T97), R126 (= R133), A183 (≠ S188), E185 (= E190), E259 (= E261), E269 (= E271), Y271 (= Y273)
7k5zA Crystal structure of argininosuccinate synthase from legionella pneumophila philadelphia 1 in complex with anppnp and a substrate analogue arginine
37% identity, 92% coverage: 12:401/425 of query aligns to 5:385/390 of 7k5zA
- active site: D15 (= D22), R95 (= R101), D124 (= D130), S176 (= S179)
- binding phosphoaminophosphonic acid-adenylate ester: A9 (= A16), Y10 (≠ F17), S11 (= S18), C37 (≠ V44), G117 (= G123), F128 (= F134)
- binding arginine: Y88 (= Y93), T92 (= T97), D124 (= D130), R127 (= R133), S185 (= S188), E187 (= E190), E261 (= E261), Y273 (= Y273)
P59846 Argininosuccinate synthase; Citrulline--aspartate ligase; EC 6.3.4.5 from Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8) (see 2 papers)
39% identity, 91% coverage: 12:399/425 of query aligns to 2:393/400 of P59846
- 6:14 (vs. 16:24, 78% identical) binding ATP
- A33 (≠ V44) binding ATP
- G114 (= G123) binding ATP
1j20A Crystal structure of thermus thermophilus hb8 argininosuccinate synthetase in complex with product (see paper)
38% identity, 91% coverage: 12:399/425 of query aligns to 2:384/386 of 1j20A
- active site: D12 (= D22), R92 (= R101), D121 (= D130), S168 (= S179)
- binding adenosine monophosphate: A6 (= A16), T13 (= T23), A33 (≠ V44), R92 (= R101), H113 (= H122), G114 (= G123), F125 (= F134)
- binding argininosuccinate: Y84 (≠ P94), T88 (= T97), A115 (≠ C124), T116 (= T125), G119 (= G128), N120 (= N129), D121 (= D130), R124 (= R133), S177 (= S188), E179 (= E190), E253 (= E261), Y265 (= Y273)
1j1zA Crystal structure of thermus thermophilus hb8 argininosuccinate synthetase in complex with substrate (see paper)
38% identity, 91% coverage: 12:399/425 of query aligns to 2:384/386 of 1j1zA
- active site: D12 (= D22), R92 (= R101), D121 (= D130), S168 (= S179)
- binding aspartic acid: A115 (≠ C124), T116 (= T125), G119 (= G128), N120 (= N129), D121 (= D130)
- binding adenosine-5'-triphosphate: A6 (= A16), T13 (= T23), A33 (≠ V44), R92 (= R101), I95 (= I104), H113 (= H122), G114 (= G123), F125 (= F134)
- binding citrulline: Y84 (≠ P94), T88 (= T97), R124 (= R133), S168 (= S179), M169 (≠ I180), S177 (= S188), E179 (= E190), E253 (= E261), Y265 (= Y273)
1kh3A Crystal structure of thermus thermophilus hb8 argininosuccinate synthetase in complex with inhibitor (see paper)
38% identity, 91% coverage: 12:399/425 of query aligns to 2:378/380 of 1kh3A
- active site: D12 (= D22), R92 (= R101), D121 (= D130), S168 (= S179)
- binding phosphoaminophosphonic acid-adenylate ester: A6 (= A16), T13 (= T23), T32 (= T43), A33 (≠ V44), H113 (= H122), G114 (= G123), F125 (= F134), S168 (= S179), M169 (≠ I180)
- binding arginine: Y84 (≠ P94), T88 (= T97), R124 (= R133), S168 (= S179), M169 (≠ I180), D170 (= D181), S177 (= S188), E179 (= E190), E253 (= E261), Y265 (= Y273)
- binding aspartic acid: A115 (≠ C124), T116 (= T125), G119 (= G128), N120 (= N129), D121 (= D130)
P00966 Argininosuccinate synthase; Citrulline--aspartate ligase; EC 6.3.4.5 from Homo sapiens (Human) (see 16 papers)
36% identity, 92% coverage: 9:398/425 of query aligns to 3:412/412 of P00966
- V64 (≠ A72) to I: in CTLN1; uncertain significance; dbSNP:rs556297791
- Y87 (= Y93) binding L-citrulline
- T91 (= T97) to P: in CTLN1; decreased affinity for aspartate; decreased affinity for citrulline; decreased argininosuccinate synthase activity; dbSNP:rs769018733
- S92 (≠ A98) binding L-citrulline
- R95 (= R101) to S: in CTLN1; increased thermal stability; loss of argininosuccinate synthase activity
- P96 (= P102) to H: in CTLN1; decreased affinity for aspartate; decreased affinity for citrulline; decreased argininosuccinate synthase activity; to L: in CTLN1; decreased thermal stability; decreased affinity for aspartate; decreased affinity for citrulline; loss of argininosuccinate synthase activity; to S: in CTLN1; no effect on thermal stability; decreased argininosuccinate synthase activity
- G117 (= G123) to S: in CTLN1; decreased thermal stability; loss of argininosuccinate synthase activity; dbSNP:rs770944877
- A118 (≠ C124) to T: in CTLN1; decreased thermal stability; decreased affinity for aspartate; decreased affinity for citrulline; decreased argininosuccinate synthase activity; dbSNP:rs775305020
- T119 (= T125) binding L-aspartate; to I: in CTLN1; decreased thermal stability; loss of argininosuccinate synthase activity
- N123 (= N129) binding L-aspartate; binding L-citrulline
- D124 (= D130) binding L-aspartate; to N: in CTLN1; loss of argininosuccinate synthase activity; dbSNP:rs936192871
- R127 (= R133) binding L-citrulline; to L: increased thermal stability; loss of argininosuccinate synthase activity; dbSNP:rs201623252; to Q: in CTLN1; increased thermal stability; loss of argininosuccinate synthase activity; dbSNP:rs201623252; to W: in CTLN1; severe clinical course; loss of argininosuccinate synthase activity; dbSNP:rs771794639
- R157 (vs. gap) to C: in CTLN1; decreased thermal stability; loss of argininosuccinate synthase activity; dbSNP:rs770585183; to H: in CTLN1; loss of argininosuccinate synthase activity; dbSNP:rs121908637
- K165 (≠ D164) modified: N6-acetyllysine; by CLOCK; mutation K->Q,R: Significant loss of acetylation but no decrease in enzyme activity; when associated with Q-176 or R-176.
- K176 (≠ A175) modified: N6-acetyllysine; by CLOCK; mutation K->Q,R: Significant loss of acetylation but no decrease in enzyme activity; when associated with Q-165 or R-165.
- W179 (= W178) to R: in CTLN1; mild; decreased affinity for aspartate; decreased affinity for citrulline; decreased argininosuccinate synthase activity; dbSNP:rs121908646
- S180 (= S179) binding L-citrulline; to I: in CTLN1; increased thermal stability; loss of argininosuccinate synthase activity; dbSNP:rs121908638; to N: in CTLN1; decreased thermal stability; decreased affinity for aspartate; decreased affinity for citrulline; decreased argininosuccinate synthase activity; dbSNP:rs121908638
- S189 (= S188) binding L-citrulline
- E191 (= E190) to Q: in CTLN1; loss of argininosuccinate synthase activity
- A192 (≠ G191) to V: in CTLN1; decreased protein abundance
- V263 (= V254) to M: in CTLN1; mild clinical course; no effect on affinity for aspartate; no effect on affinity for citrulline; decreased argininosuccinate synthase activity; dbSNP:rs192838388
- R265 (= R256) to C: in CTLN1; severe clinical course; loss of argininosuccinate synthase activity; dbSNP:rs148918985
- E270 (= E261) binding L-citrulline; to Q: in CTLN1; loss of argininosuccinate synthase activity; dbSNP:rs775163147
- R272 (= R263) to C: in CTLN1; increased thermal stability; decreased affinity for aspartate; decreased affinity for citrulline; decreased argininosuccinate synthase activity; dbSNP:rs762387914; to H: in CTLN1; increased thermal stability; decreased affinity for aspartate; decreased affinity for citrulline; decreased argininosuccinate synthase activity; dbSNP:rs768215008; to L: in CTLN1; increased thermal stability; decreased affinity for aspartate; decreased affinity for citrulline; decreased argininosuccinate synthase activity; dbSNP:rs768215008
- G280 (≠ E271) to R: in CTLN1; loss of argininosuccinate synthase activity
- Y282 (= Y273) binding L-citrulline
- T284 (≠ H275) to I: in CTLN1; mild clinical course; dbSNP:rs886039853
- M302 (≠ L293) to V: in CTLN1; no effect on affinity for aspartate; no effect on affinity for citrulline; decreased argininosuccinate synthase activity
- R304 (≠ K295) to W: in CTLN1; decreased protein abundance; dbSNP:rs121908642
- G324 (= G315) to S: in CTLN1; loss of argininosuccinate synthase activity; dbSNP:rs121908639
- G347 (= G338) to R: in CTLN1; severe clinical course
- Y359 (≠ R350) to D: in CTLN1; mild clinical course
- G362 (= G353) to V: in CTLN1; mild; no effect on affinity for aspartate; no effect on affinity for citrulline; decreased argininosuccinate synthase activity; dbSNP:rs121908647
- G390 (= G384) to R: in CTLN1; loss of argininosuccinate synthase activity; dbSNP:rs121908641
2nz2A Crystal structure of human argininosuccinate synthase in complex with aspartate and citrulline (see paper)
36% identity, 90% coverage: 13:393/425 of query aligns to 4:402/402 of 2nz2A
- active site: D13 (= D22), R92 (= R101), D121 (= D130), S176 (= S179)
- binding aspartic acid: A115 (≠ C124), T116 (= T125), G119 (= G128), N120 (= N129), D121 (= D130)
- binding citrulline: Y84 (= Y93), T88 (= T97), N120 (= N129), R124 (= R133), D178 (= D181), S185 (= S188), E187 (= E190), E266 (= E261), Y278 (= Y273)
1kp3A Crystal structure of e. Coli argininosuccinate synthetase in complex with atp and citrulline (see paper)
26% identity, 80% coverage: 12:352/425 of query aligns to 12:371/439 of 1kp3A
- active site: D22 (= D22), R106 (= R101), D135 (= D130), S191 (= S179)
- binding adenosine-5'-triphosphate: A16 (= A16), S18 (= S18), G20 (= G20), D22 (= D22), T23 (= T23), T41 (= T43), A42 (≠ V44), D127 (≠ H122), G128 (= G123), S129 (≠ C124), F139 (= F134), D193 (= D181)
- binding citrulline: Y98 (= Y93), T102 (= T97), P103 (≠ A98), T130 (= T125), G133 (= G128), N134 (= N129), D135 (= D130), R138 (= R133), D193 (= D181), T200 (≠ S188), E202 (= E190), E202 (= E190), E279 (= E261), S287 (≠ V269), Y291 (= Y273)
P0A6E4 Argininosuccinate synthase; Citrulline--aspartate ligase; EC 6.3.4.5 from Escherichia coli (strain K12) (see 4 papers)
26% identity, 80% coverage: 12:352/425 of query aligns to 13:372/447 of P0A6E4
- 17:25 (vs. 16:24, 89% identical) binding ATP
- A43 (≠ V44) binding ATP
- Y99 (= Y93) binding L-citrulline
- G129 (= G123) binding ATP
- T131 (= T125) binding ATP; binding L-aspartate
- N135 (= N129) binding L-aspartate; binding L-citrulline
- D136 (= D130) binding ATP; binding L-aspartate
- R139 (= R133) binding L-citrulline
- S192 (= S179) binding L-citrulline
- D194 (= D181) binding ATP
- T201 (≠ S188) binding L-citrulline
- E203 (= E190) binding L-citrulline
- E280 (= E261) binding L-citrulline
Sites not aligning to the query:
- 1 modified: Initiator methionine, Removed
1k97A Crystal structure of e. Coli argininosuccinate synthetase in complex with aspartate and citrulline (see paper)
26% identity, 80% coverage: 12:352/425 of query aligns to 12:371/432 of 1k97A