Align cytochrome c component of deoxyribose dehydrogenase (characterized)
to candidate RR42_RS10775 RR42_RS10775 alcohol dehydrogenase
Query= reanno::WCS417:GFF2133 (447 letters) >lcl|FitnessBrowser__Cup4G11:RR42_RS10775 RR42_RS10775 alcohol dehydrogenase Length = 434 Score = 362 bits (929), Expect = e-104 Identities = 188/437 (43%), Positives = 250/437 (57%), Gaps = 30/437 (6%) Query: 4 RRFARTAGWLAL---PCLVAAGLLAWYVTREPATPFEQEQAGATFEPALVSRGEYVARLS 60 RRF+ T + L PC AA + GA A V RG Y+A+++ Sbjct: 6 RRFSATVAFAVLLLAPCFAAAA----------------DAPGA----AQVERGRYLAKVA 45 Query: 61 DCVACHSLAGKAPFAGGLEMATPLGAIHATNITPDKSTGIGTYSLADFDRAVRHGVAPGG 120 +C ACH+ G APFAGGL + T +G +++TNITPD +GIG YS +FDRA+R GVA G Sbjct: 46 NCAACHTSVGGAPFAGGLPLKTGVGTVYSTNITPDVDSGIGAYSFEEFDRALREGVARHG 105 Query: 121 RRLYPAMPYPSYVKLSDDDIKALYAFFMQGIKPANQPNIPSDIPWPLNMRWPIALWNGVF 180 +RLYPAMPYPSY +L++ D++ALYA+ +K Q ++ WP MRW + +WN +F Sbjct: 106 KRLYPAMPYPSYARLAEPDVQALYAYLRTEVKAVRQATAEPEMRWPFGMRWLLRVWNWLF 165 Query: 181 APTATYAAKPDQDALWNRGAYIVQGPGHCGSCHTPRGLAFNEKALDEAGAPFLAGALLDG 240 + A Q WNRGAY+VQ HCG+CHTPRG+ EK LDE FLAGA ++G Sbjct: 166 LESGPVPANAGQSVEWNRGAYLVQAVAHCGACHTPRGMLMAEKGLDERSRHFLAGASVEG 225 Query: 241 WYAPSLRQDPNTGLGRWSEPQIVQFLKTGRNAHAVVYGSMTEAFNNSTQFMQDDDLAAIA 300 W + +LR DP TGLG WS I ++L TGRNAHA +G M+E +STQFM DL A+A Sbjct: 226 WASTNLRGDPRTGLGTWSREDIAEYLHTGRNAHATSFGPMSEVIASSTQFMTRPDLDAVA 285 Query: 301 RYLKSLPGDPQRDGAPWQYQAVAAVQ------DAPGAHTYATRCASCHGLDGKGQPEWMP 354 YLKS+PG + D P+ Y A A DA GA YA C CHG +GKG P Sbjct: 286 VYLKSVPG-ARSDETPYAYDAHTADALAQGRFDATGARQYAEFCMPCHGANGKGFARVFP 344 Query: 355 PLAGATSALAKESASAINITLNGSQRVVASGVPDAYRMPAFREQLSDTEIAEVLSYVRST 414 PLAG + + + +S N+ L+G+ Y MP + L + E+A VL+++R+ Sbjct: 345 PLAGNPTVVDPDPSSLANLLLDGAVTAHVGTAATDYHMPGYGWTLDNQELANVLTFIRTG 404 Query: 415 WGNNGGAVDANAVGKLR 431 WGN V V R Sbjct: 405 WGNQASQVKEATVAARR 421 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: 615 Number of extensions: 28 Number of successful extensions: 3 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: 434 Length adjustment: 32 Effective length of query: 415 Effective length of database: 402 Effective search space: 166830 Effective search space used: 166830 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 preprint 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