Align N-succinylglutamate 5-semialdehyde dehydrogenase; EC 1.2.1.71; Succinylglutamic semialdehyde dehydrogenase; SGSD (uncharacterized)
to candidate AZOBR_RS29185 AZOBR_RS29185 aldehyde dehydrogenase
Query= curated2:Q2G9T9 (471 letters) >FitnessBrowser__azobra:AZOBR_RS29185 Length = 478 Score = 208 bits (529), Expect = 4e-58 Identities = 155/429 (36%), Positives = 206/429 (48%), Gaps = 17/429 (3%) Query: 14 GAEVWRGKVGDVEEVVARARRAWPAWAAQPLATRIELVRRFANEVRKDADNLATMISRET 73 G W V EE + A A P WAA TR +++RR +E+ A+ L +++RE Sbjct: 32 GHYAW-ASVEQAEEALGAAHAALPGWAASNPQTRSDVLRRVGDELNARAEELGALLTREE 90 Query: 74 GKPLWEARTEVDSVVNKVEISIRAYADRTSQRKLDSALQG-----TAALRHKPHGVLAVL 128 GK L E EV + I YA R+ AL G TA + +P GV+ ++ Sbjct: 91 GKTLREGIGEV-----RRSAQIFHYAAGEPLRQGGEALPGLRDGTTAMVSREPVGVVVLI 145 Query: 129 GPYNFPAHLPNGHIVPALIAGNAVVFKPSEKTPATGEMLAQCFHRAGIPAAVVQVLIG-G 187 P+NFP +P AL GN VV KPSE TPA LA HRAG+PA +++G G Sbjct: 146 TPWNFPMAVPAWKTAYALAFGNTVVLKPSEVTPACAWELADILHRAGLPAGAFNLVVGDG 205 Query: 188 PEEGQALVAHDGIDGVLFTGSAHAGIAINRKLASNPGKIVALEMGGNNPIVVWDTPKIED 247 G ALV DG D V FTGS G AI + + + V LE+GG NP+VV D +E Sbjct: 206 RTLGPALV--DGADAVSFTGSPGVGRAILERSVARMTR-VQLELGGKNPLVVHDDADLEL 262 Query: 248 AATLIVQSAFTSAGQRCTAARRLIIKASMFDEVIDHVKRLADRIIVGAPFDDPAPFMGPV 307 A + +Q AF S GQRCTA R+I+ + D ++ + + VG P D A MGPV Sbjct: 263 AVDIALQGAFHSTGQRCTATSRIIVDRRVHDAFVERLVTRIAALRVGDPM-DAATDMGPV 321 Query: 308 IDNRTADGLTESFVYLLSSGGRPIKHMVRLQEDRPFLSPAIIDVTAVADRPD-VELFGPL 366 + S G R+ D FL P + T A R + E+FGP+ Sbjct: 322 VSEAQLAKDLHCIADARSEGAELAFGGGRMDGDGYFLEPTLFVGTDNAMRINRDEVFGPV 381 Query: 367 LQVVRVDDFDEAIAEANNTRFGLSASLIGGDPQDYNRFWANIRAGVVNWNRPTNGASSAA 426 V+ D D AIA AN++ LS+ ++ F RAG+V N PT G Sbjct: 382 ACVIPADGLDHAIAIANDSDHALSSGIVTRGLASAETFRRRSRAGLVMVNAPTAGIDYHV 441 Query: 427 PFGGVGLSG 435 PFGG G SG Sbjct: 442 PFGGRGPSG 450 Lambda K H 0.319 0.135 0.403 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: 594 Number of extensions: 24 Number of successful extensions: 5 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: 471 Length of database: 478 Length adjustment: 33 Effective length of query: 438 Effective length of database: 445 Effective search space: 194910 Effective search space used: 194910 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 (21.7 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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