Align 2-hydroxymuconic semialdehyde dehydrogenase; HMSD; EC 1.2.1.85 (characterized)
to candidate WP_090272859.1 BLU11_RS08070 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::P23105 (486 letters) >NCBI__GCF_900105005.1:WP_090272859.1 Length = 486 Score = 278 bits (712), Expect = 2e-79 Identities = 182/483 (37%), Positives = 261/483 (54%), Gaps = 21/483 (4%) Query: 7 FISGELVGSASGKLFDNVSPANGQVIGRVHEAGRAEVDAAVRAARAALKGPWGKMTVAER 66 +++G+ ++SG+ +PANG V+G V AEV AAV AA +AL+ W K T ER Sbjct: 17 YVNGQWQNASSGETLAVDNPANGDVLGHVPVLSAAEVGAAVDAASSALR-QWRKRTAQER 75 Query: 67 AEILHRVADGITARFGEFLEARMPGHRQAEVAGQPHRHSARRANFKVFADLLKNVANEAF 126 A+ L D + E L M + G+P S ++ A ++ A EA Sbjct: 76 ADCLLAWHD-LMLEHKEDLATLMTLEQ-----GKPLVESQGEIDYA--ASFIRWFAEEAR 127 Query: 127 EM--ATPDGAGALNYGV--RRPKGVIGVISPWNLPLLLMTWKVGPALACGNCVVVKPSEE 182 M T GA + V R+P GV I+PWN P ++T K G ALA G ++VKP+ Sbjct: 128 RMYGETIPGARIGQHIVVTRQPVGVCAAITPWNFPAAMITRKAGAALAAGCTIIVKPASA 187 Query: 183 TPLTATLLGEVMQAAGVPAGVYNVVHGFGGDSAGAFLTEHPDVDAYTFTGETGTGETIMR 242 TP +A L + + AG+P GV+NVV G G+ + LT P V +FTG T G +M Sbjct: 188 TPFSALALAVLAEEAGIPHGVFNVVTGKAGEISEV-LTRSPVVRKLSFTGSTDVGRRLMA 246 Query: 243 AAAKGVRQVSLELGGKNAGIVFADCDMDKAIEGTLRSAFANCGQVCLGTERVYVERPIFD 302 ++ +++VSLELGG IVF D D+ +A+EG + F N GQ C+ R V+ + D Sbjct: 247 QCSEHIQKVSLELGGNAPFIVFDDADISRAVEGAMVCKFRNTGQTCVCANRFLVQSGVHD 306 Query: 303 AFVARLKAGAEALKIGEPNDPEANFGPLISHKPREKVPSYYQQAVDDGATVVTGGGVPEM 362 FVA L L+IG+ +P LI+ EKV ++ A+ GA V G Sbjct: 307 KFVAALAEAMGKLRIGDGFEPGVTQSALINGDAVEKVIEHFDDAMAKGAKRVCG------ 360 Query: 363 PAHLAG-GAWVQPTIWTGLADDSAVVTEEIFGPCCHIRPFDSEEEAIELANSLPYGLASA 421 PA A G +VQP + T + + + EE FGP + FD+EEEAIELAN+ P+GLA+ Sbjct: 361 PAPDADRGNYVQPVLLTDINTNMTLCHEETFGPLAAVLRFDTEEEAIELANATPFGLAAY 420 Query: 422 IWTENVRRAHRVAGQIEAGIVWVNSWFLRDLRTAFGGSKQSGIGREGGVHSLEFYTELKN 481 ++ ++ R RVA +EAGI+ +N + + FGG K+SG+GREG H L+ YTELK Sbjct: 421 FYSRDIHRVWRVADALEAGIIGINEGLISNPMAPFGGVKESGLGREGSRHGLDEYTELKY 480 Query: 482 ICV 484 +C+ Sbjct: 481 LCM 483 Lambda K H 0.318 0.136 0.413 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: 566 Number of extensions: 29 Number of successful extensions: 4 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: 486 Length of database: 486 Length adjustment: 34 Effective length of query: 452 Effective length of database: 452 Effective search space: 204304 Effective search space used: 204304 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: 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