Align pimeloyl-CoA dehydrogenase large subunit (EC 1.3.1.62) (characterized)
to candidate H281DRAFT_00360 H281DRAFT_00360 hypothetical protein
Query= metacyc::MONOMER-20676 (396 letters) >lcl|FitnessBrowser__Burk376:H281DRAFT_00360 H281DRAFT_00360 hypothetical protein Length = 402 Score = 427 bits (1099), Expect = e-124 Identities = 212/404 (52%), Positives = 281/404 (69%), Gaps = 10/404 (2%) Query: 1 MDLNFSKEEIAFRDEVRQFFKDNVPAKTRQKLIEGRHNTKEEMVEWYRILNKKGWAVTHW 60 MDLNF+ EE AFR+EV F +D +P K+ GR T+++M W+ ILN++GW HW Sbjct: 1 MDLNFTPEEEAFREEVLAFLRDKLPQHLADKVHGGRRLTRDDMAGWHAILNERGWLANHW 60 Query: 61 PKEYGGTGWSSVQHYIFNEELQAAPAPQPLAFGVSMVGPVIYTFGSEEQKKRFLPRIANV 120 P EYGG GW++VQ +IF E A AP+ + FGV+M+GPV+ +GSE QK+ +LPRI + Sbjct: 61 PAEYGGPGWTAVQKFIFENECALAGAPRIVPFGVNMLGPVLIRYGSESQKRHWLPRILDG 120 Query: 121 DDWWCQGFSEPGSGSDLASLKTKA----EKKGDKWIINGQKTWTTLAQHADWIFCLCRTD 176 DWWCQG+SEPG+GSDLAS+KT A + G+ +I+NGQKTWTTL +A+ IFCL RT Sbjct: 121 SDWWCQGYSEPGAGSDLASVKTTAVRGVDADGEHYIVNGQKTWTTLGHYANMIFCLVRTA 180 Query: 177 PAAKKQEGISFILVDMKTKGITVRPIQTIDGGHEVNEVFFDDVEVPLENLVGQENKGWDY 236 +KQEGISF+L+DMKT G+ VRPI T+DG HEVNEVFF DV VP ENLVG+ENKGW Y Sbjct: 181 TDVRKQEGISFLLIDMKTPGVEVRPIITLDGEHEVNEVFFTDVRVPAENLVGEENKGWTY 240 Query: 237 AKFLLGNERTGIARVGMSKERIRRIKQLAAQVESGGKPVIEDPKFRDKLAAVEIELKALE 296 AK+LL ERT IA VG S + R++++AA+ + G+P+ EDP F ++A VEI+L+ ++ Sbjct: 241 AKYLLTYERTNIAGVGFSVAAVNRLRKIAAKQQRNGRPLCEDPAFAARMARVEIDLENMK 300 Query: 297 LTQLRVVADEGKHGKGKPNPASSVLKIKGSEIQQATTELLMEVIGPFAAPYDVHGDDDSN 356 T LRV+A G G P SS+LKI+G+EI+Q + L +GP+A P+ D Sbjct: 301 TTNLRVIA--AVAGGGVPGAESSMLKIRGTEIRQEISSLTRRAMGPYAQPFIEEALHDGY 358 Query: 357 ETM----DWTAQIAPGYFNNRKVSIYGGSNEIQRNIICKAVLGL 396 + + A A YFNNRK+SI+GGSNEIQ+NII K +LGL Sbjct: 359 QGAPVGPEEAASAASLYFNNRKLSIFGGSNEIQKNIISKMILGL 402 Lambda K H 0.317 0.135 0.411 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: 503 Number of extensions: 14 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: 396 Length of database: 402 Length adjustment: 31 Effective length of query: 365 Effective length of database: 371 Effective search space: 135415 Effective search space used: 135415 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: 50 (23.9 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