Align asparagine synthase (glutamine-hydrolysing) (EC 6.3.5.4) (characterized)
to candidate WP_011371822.1 SUDEN_RS00940 asparagine synthase (glutamine-hydrolyzing)
Query= BRENDA::P22106 (554 letters) >NCBI__GCF_000012965.1:WP_011371822.1 Length = 583 Score = 195 bits (496), Expect = 4e-54 Identities = 162/548 (29%), Positives = 248/548 (45%), Gaps = 124/548 (22%) Query: 1 MCSIFGVFDIKTDAVELRKKALELSRLMRHRGPDWSGIYASDNAILAHERLSIVDVNAGA 60 MC I G + E+ E+ ++HRG D+ + AH RLSI+D++ A Sbjct: 1 MCGIIG-------STEINFNHNEVLNSLKHRGEDYQNYIIQNEMFFAHTRLSIIDLDEEA 53 Query: 61 -QPLYNQQKTHVLAVNGEIYNHQALRAEYGDRYQFQTGSDCEVILALYQEKGPEFLDDLQ 119 QP+ + T L NGEIYN++ L E+ + T SD EV++ LYQ+ G +FL+ L+ Sbjct: 54 NQPMIFDEIT--LVFNGEIYNYKELIKEFS--LECVTKSDSEVLIRLYQKFGFDFLNSLE 109 Query: 120 GMFAFALYDSEKDAYLIGRDHLGIIPLYMGYDEHGQLYVASEMKALVPVCRT-------- 171 GMFAF +YD EK+ + RD G PLY Y E G+ Y ASE+KA++ + +T Sbjct: 110 GMFAFCIYDKEKNLFFCARDRFGKKPLYY-YCEKGKFYFASEIKAILKMLKTTPKLNEEA 168 Query: 172 -------------------IKEFPAGSYLWSQDGEIRSYYHRDWFDYDAVK-DNVTDKNE 211 +K+ PA SYL Q+ +I+ + D D + Sbjct: 169 LWQYLALQSPQGENTFYSGVKKLPASSYLLHQNSDIKVSTYYSLADIKITHYDEKQILKD 228 Query: 212 LRQALEDSVKSHLMSDVPYGVLLSGGLDSSIISAITKKYAARRVEDQERSEAWWPQLHSF 271 + + L D+V+ L+ DV LLSGGLDSS I+A+ K + +V H+F Sbjct: 229 VEKLLNDAVQKRLVGDVEVATLLSGGLDSSFITALYAKKSKHKV-------------HTF 275 Query: 272 AVGLPGSP---DLKAAQEVANHLGTVHHEIHFTVQEGLDAIRDVIYHIETYDVTTIRAST 328 ++G +L A+ + ++GT+HHE + E L+AI V+ H++ + A Sbjct: 276 SIGYDEHKHYCELGFAKAASEYIGTIHHEYKISKDEYLEAIEKVLEHLD--EPMADSACI 333 Query: 329 PMYLMSRKIKAMGIKMVLSGEGSDEVFGGY-------LYFH-----KAP---------NA 367 P Y++S++I G K+ LSGEGSDE F GY Y+H K P N Sbjct: 334 PTYILSKEIHNQGFKVCLSGEGSDESFLGYDNYFKMLNYYHLKNPQKTPFDLTKEWEYNN 393 Query: 368 KELHEETV-----------------RKLLA--LHMYDCA--------------------- 387 + L+ + V K +A LH Y Sbjct: 394 RRLNNQQVYQSSGETFTYAQLQRLFSKKIAPILHPYVSTYPPEQWLTYIDFSIWIAEVLM 453 Query: 388 -RANKAMSAWGVEARVPFLDKKFLDVAMRINPQDKMCGNGKMEKHILRECFEAYLPASVA 446 + ++ A +E R PFLD ++ + + K+ G K IL++ YLP S+ Sbjct: 454 TKVDRMSMAHSLELRAPFLDHHLVEYLLGVESSIKI---GDTNKAILKKIARNYLPNSII 510 Query: 447 WRQKEQFS 454 R+K+ FS Sbjct: 511 DRRKKGFS 518 Lambda K H 0.319 0.135 0.407 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 767 Number of extensions: 37 Number of successful extensions: 9 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 554 Length of database: 583 Length adjustment: 36 Effective length of query: 518 Effective length of database: 547 Effective search space: 283346 Effective search space used: 283346 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 53 (25.0 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory