SitesBLAST
Comparing WP_034273644.1 NCBI__GCF_000504245.1:WP_034273644.1 to proteins with known functional sites using BLASTp with E ≤ 0.001.
Or try Sites on a Tree, PaperBLAST, Conserved Domains, or compare to all protein structures
Found 20 (the maximum) hits to proteins with known functional sites (download)
6xppA Crystal structure of itaconate modified mycobaterium tuberculosis isocitrate lyase (see paper)
76% identity, 99% coverage: 4:428/428 of query aligns to 5:426/426 of 6xppA
- active site: Y88 (= Y91), D107 (= D110), D152 (= D154), E154 (= E156), H179 (= H181), E181 (= E183), C190 (= C192), H192 (= H194), R227 (= R229), E284 (= E286), Q307 (= Q309), S314 (= S316), S316 (= S318)
- binding 2-methylidenebutanedioic acid: W92 (= W95), C190 (= C192), H192 (= H194), R227 (= R229), N312 (= N314), S314 (= S316), S316 (= S318), T346 (= T348)
- binding magnesium ion: A275 (= A277), A278 (≠ S280), Q307 (= Q309)
7rb1A Isocitrate lyase-1 from mycobacterium tuberculosis covalently modified by 5-descarboxy-5-nitro-d-isocitric acid (see paper)
76% identity, 99% coverage: 4:428/428 of query aligns to 6:427/427 of 7rb1A
- binding dihydroxyacetic acid: Y89 (= Y91), S91 (= S93), W93 (= W95), D153 (= D154), R228 (= R229), T347 (= T348)
- binding (3E)-3-(hydroxyimino)propanoic acid: C191 (= C192), G192 (= G193), H193 (= H194), R228 (= R229), S315 (= S316), S317 (= S318), T347 (= T348)
- binding magnesium ion: A276 (= A277), A279 (≠ S280), Q308 (= Q309)
6wsiA Intact cis-2,3-epoxysuccinic acid bound to isocitrate lyase-1 from mycobacterium tuberculosis (see paper)
76% identity, 99% coverage: 4:428/428 of query aligns to 6:427/427 of 6wsiA
- active site: Y89 (= Y91), D108 (= D110), D153 (= D154), E155 (= E156), H180 (= H181), E182 (= E183), C191 (= C192), H193 (= H194), R228 (= R229), E285 (= E286), Q308 (= Q309), S315 (= S316), S317 (= S318)
- binding magnesium ion: A276 (= A277), A279 (≠ S280), Q308 (= Q309)
- binding (2R,3S)-oxirane-2,3-dicarboxylic acid: C191 (= C192), G192 (= G193), H193 (= H194), R228 (= R229), E285 (= E286), N313 (= N314), S315 (= S316), S317 (= S318), T347 (= T348)
6vb9A Covalent adduct of cis-2,3-epoxysuccinic acid with isocitrate lyase-1 from mycobacterium tuberculosis (see paper)
76% identity, 99% coverage: 4:428/428 of query aligns to 6:427/427 of 6vb9A
- active site: Y89 (= Y91), D108 (= D110), D153 (= D154), E155 (= E156), H180 (= H181), E182 (= E183), C191 (= C192), H193 (= H194), R228 (= R229), E285 (= E286), Q308 (= Q309), S315 (= S316), S317 (= S318)
- binding magnesium ion: A276 (= A277), A279 (≠ S280), Q308 (= Q309)
- binding oxalic acid: Y89 (= Y91), S91 (= S93), G92 (= G94), W93 (= W95), D153 (= D154), C191 (= C192), R228 (= R229), W283 (= W284), T347 (= T348)
5dqlA Crystal structure of 2-vinyl glyoxylate modified isocitrate lyase from mycobacterium tuberculosis (see paper)
76% identity, 99% coverage: 4:428/428 of query aligns to 6:427/427 of 5dqlA
- active site: Y89 (= Y91), D108 (= D110), D153 (= D154), E155 (= E156), H180 (= H181), E182 (= E183), C191 (= C192), H193 (= H194), R228 (= R229), E285 (= E286), Q308 (= Q309), S315 (= S316), S317 (= S318)
- binding magnesium ion: A276 (= A277), A279 (≠ S280), Q308 (= Q309)
- binding 4-hydroxy-2-oxobutanoic acid: W93 (= W95), D108 (= D110), C191 (= C192), H193 (= H194), S315 (= S316), S317 (= S318), T347 (= T348), L348 (= L349)
6c4aA Crystal structure of 3-nitropropionate modified isocitrate lyase from mycobacterium tuberculosis with pyruvate (see paper)
76% identity, 99% coverage: 4:428/428 of query aligns to 7:428/428 of 6c4aA
- active site: Y90 (= Y91), D109 (= D110), D154 (= D154), E156 (= E156), H181 (= H181), E183 (= E183), C192 (= C192), H194 (= H194), R229 (= R229), E286 (= E286), Q309 (= Q309), S316 (= S316), S318 (= S318)
- binding 3-nitropropanoic acid: Y357 (= Y357), S358 (= S358), R380 (= R380)
- binding magnesium ion: A277 (= A277), A280 (≠ S280), Q309 (= Q309)
- binding pyruvic acid: Y90 (= Y91), S92 (= S93), G93 (= G94), W94 (= W95), D154 (= D154), C192 (= C192), R229 (= R229), W284 (= W284), T348 (= T348)
P9WKK7 Isocitrate lyase; ICL; Isocitrase; Isocitratase; EC 4.1.3.1 from Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) (see 2 papers)
76% identity, 99% coverage: 4:428/428 of query aligns to 6:427/428 of P9WKK7
- SGW 91:93 (= SGW 93:95) binding substrate
- D153 (= D154) binding Mg(2+)
- C191 (= C192) mutation to S: Adopts a conformation almost identical to the wild-type.
- GH 192:193 (= GH 193:194) binding substrate
- R228 (= R229) binding substrate
- NCSPS 313:317 (= NCSPS 314:318) binding substrate
- K334 (≠ R335) modified: Isoglutamyl lysine isopeptide (Lys-Gln) (interchain with Q-Cter in protein Pup)
- T347 (= T348) binding substrate
1f8iA Crystal structure of isocitrate lyase:nitropropionate:glyoxylate complex from mycobacterium tuberculosis (see paper)
76% identity, 99% coverage: 4:428/428 of query aligns to 6:427/427 of 1f8iA
- active site: Y89 (= Y91), D108 (= D110), D153 (= D154), E155 (= E156), H180 (= H181), E182 (= E183), S191 (≠ C192), H193 (= H194), R228 (= R229), E285 (= E286), Q308 (= Q309), S315 (= S316), S317 (= S318)
- binding glyoxylic acid: Y89 (= Y91), S91 (= S93), W93 (= W95), D153 (= D154), T347 (= T348)
6lrtA Crystal structure of isocitrate lyase (caur_3889) from chloroflexus aurantiacus in complex with isocitrate and manganese ion
71% identity, 97% coverage: 14:428/428 of query aligns to 9:423/423 of 6lrtA
7cmyC Isocitrate lyase from bacillus cereus atcc 14579 in complex with magnessium ion, glyoxylate, and succinate
66% identity, 97% coverage: 14:428/428 of query aligns to 7:417/417 of 7cmyC
7rbxC Crystal structure of isocitrate lyase and phosphorylmutase:isocitrate lyase from brucella melitensis biovar abortus 2308 bound to itaconic acid (see paper)
69% identity, 95% coverage: 24:428/428 of query aligns to 14:423/425 of 7rbxC
P0A9G6 Isocitrate lyase; ICL; Isocitrase; Isocitratase; EC 4.1.3.1 from Escherichia coli (strain K12) (see 3 papers)
65% identity, 99% coverage: 6:428/428 of query aligns to 2:434/434 of P0A9G6
- SGW 91:93 (= SGW 93:95) binding substrate
- D157 (= D154) binding Mg(2+)
- C195 (= C192) active site, Proton acceptor; mutation to A: Large decrease in activity.; mutation to S: Large decrease in activity.
- A219 (= A216) mutation to C: Isocitrate lyase activity is reduced compared to the wild-type.
- R232 (= R229) binding substrate
Sites not aligning to the query:
- 1 modified: Initiator methionine, Removed
1igwC Crystal structure of the isocitrate lyase from the a219c mutant of escherichia coli (see paper)
64% identity, 95% coverage: 6:411/428 of query aligns to 1:415/416 of 1igwC
- active site: Y88 (= Y91), D107 (= D110), D156 (= D154), E158 (= E156), H183 (= H181), E185 (= E183), C194 (= C192), R231 (= R229), E288 (= E286), K311 (≠ Q309), S318 (= S316), S320 (= S318)
- binding pyruvic acid: S90 (= S93), G91 (= G94), W92 (= W95), D156 (= D154), R231 (= R229), T350 (= T348)
1igwA Crystal structure of the isocitrate lyase from the a219c mutant of escherichia coli (see paper)
60% identity, 95% coverage: 6:411/428 of query aligns to 1:395/396 of 1igwA
- active site: Y88 (= Y91), D107 (= D110), D156 (= D154), E158 (= E156), H183 (= H181), E185 (= E183), C194 (= C192), R227 (= R229), E284 (= E286), K307 (≠ Q309)
- binding pyruvic acid: S90 (= S93), W92 (= W95), D156 (= D154), R227 (= R229), T330 (= T348)
5e9gD Structural insights of isocitrate lyases from magnaporthe oryzae (see paper)
35% identity, 94% coverage: 1:404/428 of query aligns to 11:478/486 of 5e9gD
- active site: Y100 (= Y91), D119 (= D110), D173 (= D154), D175 (≠ E156), H200 (= H181), E202 (= E183), C211 (= C192), H213 (= H194), R248 (= R229), E363 (= E286), Q386 (= Q309), S393 (= S316), S395 (= S318)
- binding glyoxylic acid: Y100 (= Y91), S102 (= S93), G103 (= G94), W104 (= W95), D173 (= D154), H200 (= H181), R248 (= R229), T424 (= T348)
- binding glycerol: C211 (= C192), G212 (= G193), H213 (= H194), R248 (= R229)
5e9fD Structural insights of isocitrate lyases from magnaporthe oryzae (see paper)
36% identity, 94% coverage: 1:404/428 of query aligns to 10:446/453 of 5e9fD
- active site: Y99 (= Y91), D118 (= D110), D172 (= D154), D174 (≠ E156), H199 (= H181), E201 (= E183), R240 (= R229), E330 (= E286), Q353 (= Q309), S360 (= S316), S362 (= S318)
- binding magnesium ion: D118 (= D110), D172 (= D154)
7ebeA Crystal structure of isocitrate lyase-1 from candida albicans (see paper)
37% identity, 58% coverage: 9:257/428 of query aligns to 16:275/544 of 7ebeA
- active site: Y99 (= Y91), D118 (= D110), D172 (= D154), D174 (≠ E156), H199 (= H181), E201 (= E183), C210 (= C192), H212 (= H194), R247 (= R229)
- binding magnesium ion: G102 (= G94), W103 (= W95), D172 (= D154)
Sites not aligning to the query:
6edwC Crystal structure of mycobacterium tuberculosis icl2 in the apo form (see paper)
39% identity, 54% coverage: 24:252/428 of query aligns to 22:264/724 of 6edwC
Sites not aligning to the query:
6edwB Crystal structure of mycobacterium tuberculosis icl2 in the apo form (see paper)
39% identity, 54% coverage: 24:252/428 of query aligns to 22:264/746 of 6edwB
Sites not aligning to the query:
6edzA Crystal structure of mycobacterium tuberculosis icl2 in complex with acetyl-coa, form i (see paper)
39% identity, 54% coverage: 24:252/428 of query aligns to 22:264/733 of 6edzA
Sites not aligning to the query:
- active site: 437, 460, 467, 469
- binding acetyl coenzyme *a: 643, 644, 645, 646, 652, 653, 655, 657, 658, 679, 681, 682, 684, 688, 692, 732
Query Sequence
>WP_034273644.1 NCBI__GCF_000504245.1:WP_034273644.1
MTDTTKSREQAAAELAKEWETNPRWKGIDRSYTAEDVVKLRGSVIEENTLARRGAEKLWD
LLHTEDYVHALGALTGGQAVQQVRAGLKAIYLSGWQVAADANLAGQTYPDQSLYPANSVP
AVVRRINNALGRADQINYAEGNTDIDWYAPIVADAEAGFGGPLNAFELMKGMIAAGAAGV
HWEDQLASEKKCGHLGGKVLVPTKQHVRTLNAARLASDVSDVPSIVIARTDAEAATLMTS
DVDERDEKFLTGERTSEGFYKVRNGIEPCIERAKAYAPYSDLIWMETGTPDLEVARQFAE
AVKAEFPDQMLAYNCSPSFNWRKNLDDATIAKFQRELGHMGYKFQFITLAGFHALNYSMF
DLAYGYAREGMTAYVDLQDREFASEERGFTAVKHQREAGTGWFDLVSTAINPESSTTALT
GSTEEAQF
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SitesBLAST's Database
SitesBLAST's database includes
(1) SwissProt
entries with experimentally-supported functional features;
and (2) protein structures with bound ligands, from the
BioLip database.
by Morgan Price,
Arkin group
Lawrence Berkeley National Laboratory