Align cytochrome c component of deoxyribose dehydrogenase (characterized)
to candidate H281DRAFT_02833 H281DRAFT_02833 Cytochrome c, mono- and diheme variants
Query= reanno::WCS417:GFF2133 (447 letters) >FitnessBrowser__Burk376:H281DRAFT_02833 Length = 438 Score = 338 bits (868), Expect = 2e-97 Identities = 187/434 (43%), Positives = 249/434 (57%), Gaps = 29/434 (6%) Query: 21 AGLLAWYVTREPATPFEQE-QAGATFEPALVSRGEYVARLSDCVACHSLAGKAPFAGGLE 79 +G AW + P F Q+ +A + AL+ RGEY+A DC+ACH+ A PFAGGL Sbjct: 11 SGAFAWS-SALPVCAFAQDAKAVDGNDAALIKRGEYLATAGDCMACHTTAKGKPFAGGLP 69 Query: 80 MATP-LGAIHATNITPDKSTGIGTYSLADFDRAVRHGVAPGGRRLYPAMPYPSYVKLSDD 138 + P LG I+++NITPD TGIGT+SL DFDRA+R GV+ G LYPAMPY SY K+SD Sbjct: 70 LKVPMLGTIYSSNITPDPQTGIGTWSLEDFDRALRKGVSKDGHNLYPAMPYVSYAKVSDG 129 Query: 139 DIKALYAFFMQGIKPANQPNIPSDIPWPLNMRWPIALWNGVFAPTATYAAKPDQDALWNR 198 D+KALYA+F G+ P Q SDI WPLNMRWP+ +WN +F + Y AKP Q A WNR Sbjct: 130 DVKALYAYFRYGVVPVQQATRASDIAWPLNMRWPLTVWNWMFLKSGPYQAKPQQSAEWNR 189 Query: 199 GAYIVQGPGHCGSCHTPRGLAFNEKALDEAGAPFLAGALLDGWYAPSLRQDPNTGLGRWS 258 GAY+VQG HC +CHTPRG A E+ALDE G+ FL G++L W ++ P++G+G WS Sbjct: 190 GAYLVQGLAHCSTCHTPRGFAMQEQALDETGSGFLGGSVLADWDGYNITSSPDSGIGGWS 249 Query: 259 EPQIVQFLKTGR-NAHAVVYGSMTEAFNNSTQFMQDDDLAAIARYLKSLPGDPQRDGAPW 317 Q+VQ+L+TG A G M EA +S M D D+ AIA Y++++P P DG Sbjct: 250 HTQLVQYLQTGSVPGLAQAAGPMAEAVEHSFSKMSDADIGAIATYVRTVP--PVNDGGAQ 307 Query: 318 QYQAVAAVQDAPG------------------AHTYATRCASCHGLDGKGQPE-WMPPLAG 358 + P A Y CA+CH GKG P+ + PPL Sbjct: 308 SGSRSRSAWGKPSTDVARLRGVAMNDGTLDPARLYLGNCATCHQASGKGTPDGYYPPLLH 367 Query: 359 ATSALAKESASAINITLNGSQRVVASGVPDAYRMPAFREQLSDTEIAEVLSYVRSTWGNN 418 ++ A + + + L+G QR A + MPAF QL+D +IA + +YV + +GN Sbjct: 368 NSTVGASNPGNLMQVILHGVQRKAAG---NDVGMPAFAAQLNDAQIAALTNYVTTQFGNP 424 Query: 419 GG-AVDANAVGKLR 431 V V +LR Sbjct: 425 AAQRVSEKDVARLR 438 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: 666 Number of extensions: 47 Number of successful extensions: 9 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: 438 Length adjustment: 32 Effective length of query: 415 Effective length of database: 406 Effective search space: 168490 Effective search space used: 168490 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