Align cytochrome c component of deoxyribose dehydrogenase (characterized)
to candidate H281DRAFT_01762 H281DRAFT_01762 Cytochrome c, mono- and diheme variants
Query= reanno::WCS417:GFF2133 (447 letters) >FitnessBrowser__Burk376:H281DRAFT_01762 Length = 450 Score = 379 bits (972), Expect = e-109 Identities = 202/439 (46%), Positives = 263/439 (59%), Gaps = 15/439 (3%) Query: 5 RFARTAGWLALPCLVAAGLLAWYVTREPATPFEQEQAGATFEPALVSRGEYVARLSDCVA 64 R A TA L L + A L A + + + + E + + +PAL+SRG Y+A+L DC Sbjct: 10 RAAFTAFALTLAMTMVAALCAHSLAQSDSPSVDDEVSLS--DPALISRGAYLAKLGDCAG 67 Query: 65 CHSLAGK-APFAGGLEMATPLGAIHATNITPDKSTGIGTYSLADFDRAVRHGVAPGGRRL 123 CH++ + APFAGGL M +P G I++TNITPD TGIG YS ADF+RA+R GVAPGG+RL Sbjct: 68 CHTVPKQGAPFAGGLPMGSPFGTIYSTNITPDPQTGIGRYSYADFERALRDGVAPGGKRL 127 Query: 124 YPAMPYPSYVKLSDDDIKALYAFFMQGIKPANQPNIPSDIPWPLNMRWPIALWNGVFAPT 183 YPAMPY S+ K++D D+ ALYA+FM G++P + +P+P + RW +A W+ F Sbjct: 128 YPAMPYASFTKINDSDMHALYAYFMHGVQPVAHRPPETKLPFPFSQRWGLAFWDFAFVQH 187 Query: 184 ATYAAKPDQDALWNRGAYIVQGPGHCGSCHTPRGLAFNEKALDEAGAPFLAGALLDGWYA 243 + +DALWNRGAYIVQ GHCG+CHTPRG F E+ DE+ +L G D W+A Sbjct: 188 ERFIPDGKRDALWNRGAYIVQSLGHCGACHTPRGPGFEERGYDESSKLYLTGGTNDHWFA 247 Query: 244 PSLRQDPNTGLGRWSEPQIVQFLKTGR--NAHAVVYGSMTEAFNNSTQFMQDDDLAAIAR 301 P+L DP +GLGR S I FLK+G + H V +GSM E +S Q+ DDDL A+AR Sbjct: 248 PNLTGDPGSGLGRLSPRDIASFLKSGHGVDVHVVTFGSMVEVVEDSGQYFSDDDLNAVAR 307 Query: 302 YLKSLPGDPQRDGA------PWQYQAV---AAVQDAPGAHTYATRCASCHGLDGKGQPEW 352 YLKSLP Q GA Q AV A + PGA Y + CA CH DG+G+P Sbjct: 308 YLKSLPA-RQSSGAYKPNTQKLQETAVSLKAGEVERPGAGLYMSFCAKCHQADGRGEPHK 366 Query: 353 MPPLAGATSALAKESASAINITLNGSQRVVASGVPDAYRMPAFREQLSDTEIAEVLSYVR 412 P LAG + LA +++S I + L G P MPAFR Q +D EIA VLS+VR Sbjct: 367 FPALAGNPAVLAPDTSSLIRLVLEGGTSPQTENGPIHREMPAFRNQFTDREIARVLSFVR 426 Query: 413 STWGNNGGAVDANAVGKLR 431 + WGN V V +R Sbjct: 427 TAWGNEARPVATRDVSTVR 445 Lambda K H 0.318 0.133 0.423 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: 693 Number of extensions: 38 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: 447 Length of database: 450 Length adjustment: 33 Effective length of query: 414 Effective length of database: 417 Effective search space: 172638 Effective search space used: 172638 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 (21.7 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