Align 4-hydroxybutyrate-CoA ligase (EC 6.2.1.40) (characterized)
to candidate WP_084199459.1 C0029_RS10005 long-chain fatty acid--CoA ligase
Query= BRENDA::A4YDR9 (549 letters) >NCBI__GCF_002869505.1:WP_084199459.1 Length = 511 Score = 230 bits (586), Expect = 1e-64 Identities = 160/508 (31%), Positives = 246/508 (48%), Gaps = 28/508 (5%) Query: 37 DKTAVVYRDSRYTYSTFYDNVMVQASALMRRGFSREDKLSFISRNRPEFLESFFGVPYAG 96 D+ AVV+ + TY+ F D V QA L G D++ ++ N P LE+ F G Sbjct: 23 DRIAVVFEEQEITYAEFADRVRRQAQLLRDAGVCVGDRVGYLGFNHPALLETLFATQALG 82 Query: 97 GVLVPINFRLSPKEMAYIINHSDSKFVVVDEPYLNSLLEVKDQIKAEIILLEDPDNPSAS 156 + VP+NFRL+ +E+ +IIN + +VVD+ + D++ + + Sbjct: 83 AIFVPLNFRLTAEELTFIINDAGVHSLVVDDALRPVVEPALDKLCCRRYFSSESEADGWR 142 Query: 157 ETARKEVRMTYRELVKGGSRDPLPIP-AKEEYSMITLYYTSGTTGLPKGVMHHHRGAFLN 215 + + +PL A +++ + YTSGTTGLPKG M H N Sbjct: 143 HLSSERAAC-----------EPLTSTVAVDQHETGLIMYTSGTTGLPKGAMLTHGNFVWN 191 Query: 216 AMAEVLEHQMDLNSVYLWTLPMFHAASWG-FSWATVAVGATNVCLDKVDYPLIYRLVEKE 274 + + +++ L P+FH + + +G+ V L D + E+ Sbjct: 192 NINASMAFGASRDNIILTAAPLFHIGGLNVMTLHSFHLGSKLVLLRNFDPAAVLENFERY 251 Query: 275 RVTHMCAAPTVYVNLADYMKRNNLKFSNRVHMLVAGAAPAPATL-KAMQEIGGYMCHVYG 333 +VTHM AP +Y+ +A + + S+ + +LV GAAP P +L + G C YG Sbjct: 252 KVTHMFGAPAMYLFMAQLPQFADTDLSS-LDVLVCGAAPVPESLIETYGARGVSFCQGYG 310 Query: 334 LTETYGPHSICEWRREWDSLPLEEQAKLKARQGIPYVSFEMDVFDANGKPVPWDGKTIGE 393 LTET P S P +KL + +P S + DA+ +P+P K GE Sbjct: 311 LTET-APFSAL-------LTPEHAVSKLGSAGQVPLYSGTR-IVDADNQPLPAGEK--GE 359 Query: 394 VVMRGHNVALGYYKNPEKTAESF-RDGWFHSGDAAVVHPDGYIEIVDRFKDLINTGGEKV 452 + +RG N+ GY+ PE TA + +GWFHSGD + +G++ I DR KD++ +GGE V Sbjct: 360 ICLRGPNIMKGYWNRPEATASAIDSEGWFHSGDIGYLDDEGFLYICDRLKDMVISGGENV 419 Query: 453 SSILVEKTLMEIPGVKAVAVYGTPDEKWGEVVTARIELQEGVKLTEEEVIKFCKERLAHF 512 VE L + + VAV GTPDEKWGE VTA + L EG LT E + +F LA + Sbjct: 420 YPAEVEGVLYKHEAIAEVAVIGTPDEKWGEAVTAVVALHEGASLTLEGLREFADPFLARY 479 Query: 513 ECPKIVE-FGPIPMTATGKMQKYVLRNE 539 + P +E +P GK+ K+VL+ + Sbjct: 480 KLPLRMEVVEALPRNPAGKVLKFVLKEQ 507 Lambda K H 0.319 0.136 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: 666 Number of extensions: 31 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 549 Length of database: 511 Length adjustment: 35 Effective length of query: 514 Effective length of database: 476 Effective search space: 244664 Effective search space used: 244664 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 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