Align Succinylglutamic semialdehyde dehydrogenase (EC 1.2.1.71) (characterized)
to candidate WP_007152862.1 MDG893_RS06100 2-hydroxymuconic semialdehyde dehydrogenase
Query= reanno::SB2B:6938906 (486 letters) >NCBI__GCF_000170835.1:WP_007152862.1 Length = 486 Score = 190 bits (482), Expect = 1e-52 Identities = 159/479 (33%), Positives = 231/479 (48%), Gaps = 31/479 (6%) Query: 4 FINGQWL-AGEGKEMQSKNPANGEVIWQGKAAVPAQVQAAVMAARDA-QFEWFMLGFEGR 61 +INGQ++ + GK + NPANG+VI + A +V AAV AA+ A + W + E R Sbjct: 7 YINGQYVGSASGKLFDNVNPANGQVISKVHEAGREEVDAAVKAAKSALRGPWGKMTLEER 66 Query: 62 QAIVEAYRNELEANKAELAEVIAQETGKPRWETATEAAAMIGKIGLSVSA-YHKRTGTEV 120 I+ + + A E E +TGKPR A+ G V A K TE Sbjct: 67 TGILHKVADGINARFEEFLEAECLDTGKPR-SLASHIDIPRGAANFKVFADMIKNVPTES 125 Query: 121 NE-------GAAGRAVLRHKPHGVVAVFGPYNFPGHLPNGHIVPALLAGNTVVFKPSELT 173 E GA AV R P GV+ V P+N P L + PAL GNTVV KPSE T Sbjct: 126 FEMPTPDGTGALNYAVRR--PKGVIGVISPWNLPLLLMTWKVGPALACGNTVVVKPSEET 183 Query: 174 PKVAELMLKLWEKAGLPAGVINLVQ--GEVETGKALASHPQLDGLFFTGSSRTGHLLHQQ 231 P L+ + + AG+P GV N+V G G L HP +DG FTG + TG ++ + Sbjct: 184 PTTTALLGDVMKDAGVPDGVFNVVHGFGGDSAGAFLTEHPMVDGFTFTGETGTGEVI-MK 242 Query: 232 YAGHPGKILALEMGGNNPLIVKGVSDTRAAIHDIIQSAFISSGQRCTCARRLYVEKGAEG 291 A + ++LE+GG N +V D AI ++SAF + GQ C R+YVE+ Sbjct: 243 AAAKGIRDISLELGGKNAGLVFADCDMDKAIEGTMRSAFANCGQVCLGTERVYVERSI-F 301 Query: 292 DKLLAGLVEAVKAIKVGPWNADPQPFMGSMISETAAKGMLDAQRNLLNLGAK-----SLV 346 D+ + L EA + IK+GP + D + MG ++S + +L + ++ GA + Sbjct: 302 DEFVGRLKEAAEGIKIGPPD-DIEADMGPLVSLKHREKVLSYYQKAVDDGATLVTGGGVP 360 Query: 347 EMTHLQAGTGLVSP----GLIDVTEVIELPDEEYFGPLLQVVRYTSFDEAIRLANDTRYG 402 EM AG V P GL + + VI +E FGP + + + + +EAI LAN YG Sbjct: 361 EMPEALAGGAWVQPTIWTGLPEDSAVI---TDEIFGPCVHLCPFDNEEEAIELANSLPYG 417 Query: 403 LSAGILADDKADYEYFLARIRAGIVNWNKQITGASGAAPFGGVGASGNHRASAFYAADY 461 L++ I +++ +I AGI+ W PFGG SG R ++ ++ Sbjct: 418 LASAIWSENITRAHRVAGQIEAGII-WVNSWFLRDLRTPFGGSKQSGIGREGGVHSLEF 475 Lambda K H 0.317 0.133 0.393 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: 599 Number of extensions: 40 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: 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 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 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