Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate WP_106709897.1 CU102_RS04990 aldehyde dehydrogenase
Query= curated2:Q1QTQ7 (489 letters) >NCBI__GCF_003010955.1:WP_106709897.1 Length = 505 Score = 196 bits (499), Expect = 1e-54 Identities = 164/499 (32%), Positives = 238/499 (47%), Gaps = 27/499 (5%) Query: 1 MQAKQQLLIDGAWVDGDAA-RFAKTDPVSGETLWTATAASATQVEHAVAAARQAFPD--W 57 +Q IDGA+ ++ RF T+P +GETL A A+ V+ AV ARQAF D W Sbjct: 17 IQFPTNAFIDGAFRPANSGKRFRTTNPATGETLAEIAACDASDVDFAVGKARQAFDDGRW 76 Query: 58 ARRSFAERQAVVERFRECLETHREHLATAIAQETGKPLWEART-EVGAMIGKVAISITAY 116 +S AER+AV+ F + LE HR LA + ++GKP+ E +T +V I + Sbjct: 77 HLQSPAERKAVLINFAKLLERHRHELAVMESLDSGKPVRECQTVDVPDTIHTLRWHAELI 136 Query: 117 HERTGERARDIGDARAVLRHRPHGVLAVYGPYNFPGHLPNGHIVPALLAGNAVVFKPSEQ 176 + A +A ++ P GV+ P+NFP + I PAL AG +V+ KP+++ Sbjct: 137 DKLYDNTAPVGSNALTMVVREPVGVVGCVLPWNFPLLMLAWKIGPALAAGCSVIVKPAQE 196 Query: 177 TPMTADLTLQCWLEAGLPAGVINLVQGAA-EVGQALAGSADIDGLLFTGSAKVGGLLHRQ 235 T T + EAG+PAGV N+V G EVG+ + D+D + FTGS G R Sbjct: 197 TTPTTLRVAELAHEAGIPAGVFNVVPGGGKEVGEPIGMHMDVDMVAFTGSTPTGRRFLRY 256 Query: 236 FGGQVDKILALELGGNNPLVV-KDVPDREAAVLSILQSAFASGGQRCTCARRLIVPHGAV 294 K + LE GG NP VV D D + I+ AF + G+ C+ RLIV H +V Sbjct: 257 AADSNLKRVVLECGGKNPAVVLDDAEDLDLVAEQIVNGAFWNMGENCSATSRLIV-HASV 315 Query: 295 GDDLIDALTSAIAELRVAAPFSEPAPFYAGLTSVEAADGLLAAQDDL------VARGGRP 348 D+L++ + + + E + P +P L S D + + D + VA GG Sbjct: 316 KDELLERIGAYMREWKTGDPL-DPENRIGTLVSKNHFDKVSSFLDSVKSEKLSVAHGG-- 372 Query: 349 LSRMRRLQAGTSLLSPGLID--VTGCDVPDEEHFGPLLKVHRYRDWDEAIALANDTRYGL 406 Q G + P ++D + EE FGP+L V + EA+ALANDT YGL Sbjct: 373 -----ETQKGI-YIEPTVVDGVTPASRLFQEEIFGPILSVTTFNSLAEAVALANDTNYGL 426 Query: 407 SAGLIGGERADWDDFLLRIRAGIVNWNRQTTGASSDAPFGGIGDSG-NHRPSAYYAAD-Y 464 +A + IRAG+V N G + PFGG +SG R + +A D Y Sbjct: 427 TASVYTASLRKAIKLSREIRAGLVTVNCFGEG-DATTPFGGYKESGFGGRDKSVFAHDNY 485 Query: 465 CAYPVASMEAETLVLPETL 483 C ++ + ET+ Sbjct: 486 CELKTIWIDVSDRSVDETV 504 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: 623 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: 505 Length adjustment: 34 Effective length of query: 455 Effective length of database: 471 Effective search space: 214305 Effective search space used: 214305 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 Sep 24 2021. 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