Align Succinylglutamic semialdehyde dehydrogenase (EC 1.2.1.71) (characterized)
to candidate WP_017549863.1 C792_RS0112845 aldehyde dehydrogenase family protein
Query= reanno::MR1:199807 (487 letters) >NCBI__GCF_000330705.1:WP_017549863.1 Length = 488 Score = 197 bits (501), Expect = 7e-55 Identities = 148/485 (30%), Positives = 233/485 (48%), Gaps = 20/485 (4%) Query: 1 MTHFIKGQWHTGKGHDVASS-NPANG-EIIWRGQTATAEQVNAAVDAAREAQFDWFILGF 58 + +FI G W T G ++ NPAN E++ +T+E ++ A+D+A + W + Sbjct: 9 LKNFINGTWTTPSGKELKQGVNPANTKEVVSSFYQSTSEDLSDAIDSASKGFQQWKDIPA 68 Query: 59 DARLKIVEAYRSQLEANKAELAETIAQETGKPQWETATEVAAMIGKIGLSASAYNKRTGT 118 R + + + +E K +LA+T+ QE GK + EV G + A + G+ Sbjct: 69 PQRGEYLYKISALMEEEKDDLAKTMVQEEGKTYNDAIKEVGYAAGIVKYYAGECRRLKGS 128 Query: 119 ETN-DTPAGRAVLRHKPHGVVAVFGPYNFPGHLPNGHIVPALLAGNSVVFKPSELTPKVA 177 D P + + +P GVV V P+NFP +P PAL +GN+VV KPS TP Sbjct: 129 ILEADMPDIQIQTKPEPLGVVLVVTPWNFPLSIPAWKTAPALASGNAVVLKPSSETPLTV 188 Query: 178 ELMVTLWEKSGLPAGVLNLVQGEVDTGKALASHPQLDGLFFTGSSRTGHLLHQQYAGHPG 237 + + +++G+PAGV+N V + HP + + FTGS+ G ++ + A Sbjct: 189 MKFMDIIQRAGVPAGVVNSVIAPGKLVSEMIHHPAVKAVTFTGSNTVGEKIYAEAAKGMK 248 Query: 238 KILALEMGGNNPLIIKGVADIKAAVHDILQSAYISSGQRCTCARRLYVEQGEQGDALVAK 297 + L LEMGG NPLII ADI AV + Y +GQ CT R+ V + + K Sbjct: 249 RCL-LEMGGKNPLIIMEDADIDEAVQIAVTGGYGQTGQACTATGRIIVHE-KVVKEFTEK 306 Query: 298 LVEAVKQIKVGPWNAQPQPF-MGSMISEAAAKGMV-------AAQANLLSLGGVPLVELM 349 LV+ +Q+KVG N + MG +S+A + + A +L+ GG+P + Sbjct: 307 LVKRTEQLKVG--NGMHEGIDMGPQVSQAERQSTLDLIQSAKDEGATVLTGGGIP--QYP 362 Query: 350 HLQAGTGLVSPGLIDVTAVSELPDEEYFGPLLQLVRYSDFDQAIKLANQTRYGLSAGILA 409 L+ G + + +V + +E FGP+ ++ D D+AI +AN YGLS+ I Sbjct: 363 ELEDGYFIEPTVISNVKPAMTISQKEVFGPVNSIIEVRDIDEAISVANDVEYGLSSAICT 422 Query: 410 DSREDYEYFLARIRAGIVNWNKQITGASGAAPFGGV--GASGNHRASAFYAAD-YCAYPV 466 + L+ I AGIV N TG APFGG ++G ++ D YC Y Sbjct: 423 RNIGYMNKALSEIEAGIVKVNMTTTGTFFQAPFGGYKKSSTGTYKELGSEGMDFYCQYKT 482 Query: 467 ASVEA 471 +++ Sbjct: 483 RYIKS 487 Lambda K H 0.316 0.133 0.391 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: 581 Number of extensions: 35 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: 487 Length of database: 488 Length adjustment: 34 Effective length of query: 453 Effective length of database: 454 Effective search space: 205662 Effective search space used: 205662 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