Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate WP_041376699.1 PNAP_RS13165 NAD-dependent succinate-semialdehyde dehydrogenase
Query= curated2:Q1QTQ7 (489 letters) >NCBI__GCF_000015505.1:WP_041376699.1 Length = 490 Score = 192 bits (487), Expect = 3e-53 Identities = 146/472 (30%), Positives = 223/472 (47%), Gaps = 26/472 (5%) Query: 4 KQQLLIDGAWVDGDAARFAKTDPVSGETLWTATAASATQVEHAVAAARQAFPDWARRSFA 63 K LI+G W+ G A+RF +DP +G L E A+AAA A+P W ++ Sbjct: 18 KTDALINGQWLAG-ASRFDVSDPSNGNKLADVANLGPADAEAAIAAANAAWPAWRGKTGK 76 Query: 64 ERQAVVERFRECLETHREHLATAIAQETGKPLWEARTEVGAMIGKVAISITAYHERTGER 123 ER ++ ++ + L ++E LA + E GKP EA+ EV V GE Sbjct: 77 ERSIILRKWFDLLMANQEDLARIMTAEQGKPFAEAKGEVAYGASFVEWFAEEAKRVNGET 136 Query: 124 ARDI-GDARAVLRHRPHGVLAVYGPYNFPGHLPNGHIVPALLAGNAVVFKPSEQTPMTAD 182 + R ++ +P GV P+NFP + + PAL AG VV KP+E TP+TA Sbjct: 137 LPQFDNNRRLMVLKQPIGVCVAITPWNFPLAMITRKVAPALAAGCTVVIKPAELTPLTAL 196 Query: 183 LTLQCWLEAGLPAGVINLV--QGAAEVGQALAGSADIDGLLFTGSAKVGGLLHRQFGGQV 240 ++ + AG+P+GV+N++ +A VG+ S + + FTGS +VG +L Q + Sbjct: 197 AAVELAVRAGVPSGVLNILTTDESAAVGKVFCASDVVRHISFTGSTEVGRILMAQSAPSI 256 Query: 241 DKILALELGGNNPLVVKDVPDREAAVLSILQSAFASGGQRCTCARRLIVPHGAVGDDLID 300 K L+LELGGN P +V D D ++AV + S + + GQ C CA R+ V G V D + Sbjct: 257 KK-LSLELGGNAPFIVFDDADIDSAVEGAMASKYRNAGQTCVCANRIYVQEG-VYDQFVH 314 Query: 301 ALTSAIAELRVAAPFSEPAPFYAGLTSVEAADGLLAAQDDLVARGGRPLSRMRRLQAGTS 360 + L+V F E L A + D +A+GG+ L+ +L+ Sbjct: 315 KFAEKVRLLKVGNGF-EDGVGQGPLIEDAAVHKVERHVQDALAKGGKLLAGGHKLEG--Q 371 Query: 361 LLSPGLIDVTGCDV--PDEEHFGPLLKVHRYRDWDEAIALANDTRYGLSA-------GLI 411 P +I D+ EE FGP V R+ EAI AN+T +GL++ G I Sbjct: 372 FFEPTVISEAHADMLCAREETFGPFAPVFRFTHEQEAIDAANNTEFGLASYFYSRDIGRI 431 Query: 412 GGERADWDDFLLRIRAGIVNWNRQTTGASSDAPFGGIGDSGNHRPSAYYAAD 463 + ++ I AG++ A+ PFGG+ SG R + + + Sbjct: 432 YRVAEALEYGMVGINAGVI--------ATEHVPFGGVKQSGLGREGSSHGME 475 Lambda K H 0.319 0.135 0.409 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: 583 Number of extensions: 28 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 489 Length of database: 490 Length adjustment: 34 Effective length of query: 455 Effective length of database: 456 Effective search space: 207480 Effective search space used: 207480 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: 52 (24.6 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