Align 4-hydroxybutyrate-CoA ligase (AMP-forming) (EC 6.2.1.40) (characterized)
to candidate CCNA_00192 CCNA_00192 long-chain-fatty-acid--CoA ligase
Query= BRENDA::A4YDR9 (549 letters) >FitnessBrowser__Caulo:CCNA_00192 Length = 539 Score = 224 bits (570), Expect = 9e-63 Identities = 152/502 (30%), Positives = 246/502 (49%), Gaps = 14/502 (2%) Query: 47 RYTYSTFYDNVMVQASALMRRGFSREDKLSFISRNRPEFLESFFGVPYAGGVLVPINFRL 106 RY Y+ A AL R G D+++ ++ N LE F+ P G VL N RL Sbjct: 40 RYDYAGLAGRAAQAAHALRRLGIKAGDRVTSLAWNTHRHLELFYAAPGIGAVLHTANPRL 99 Query: 107 SPKEMAYIINHSDSKFVVVDEPYLNSLLEVKDQIKA--EIILLEDPDNPSASETARKEVR 164 +++ Y INH++S + + + + + Q+ ++L D + Sbjct: 100 FDEQIVYTINHAESGVLFFERNFQALVERIAPQLTTVKTFVMLSDAERTVPGAVGA---- 155 Query: 165 MTYRELVKGGSRDPLPIPAKEEYSMITLYYTSGTTGLPKGVMHHHRGAFLNAMAEVLEHQ 224 ++Y L++G D + P+ +E + L YTSGTTG PKGV++ HR L+AMA L Sbjct: 156 ISYETLIEG-EPDVIAWPSFDENAGAFLCYTSGTTGDPKGVLYSHRAVVLHAMAGGLNSA 214 Query: 225 MDLN--SVYLWTLPMFHAASWGFSWATVAVGATNVC-LDKVDYPLIYRLVEKERVTHMCA 281 V + ++HA +WG ++ GA V DK+D +++L+E E VT Sbjct: 215 FGFTPFDVVMPCSSLYHATAWGLPFSAPICGAKLVLPADKMDGASLHQLIEGEGVTFTGG 274 Query: 282 APTVYVNLADYMKRNNLKFSNRVHMLVAGAAPAPATLKAMQE-IGGYMCHVYGLTETYGP 340 PT++ D++ +N+ + + +++ G+A A + + G ++G+TET Sbjct: 275 VPTIWTMYLDWLDKNDRRPDSLKKVVIGGSAVPRAMAETFKRRYGVQTLQIWGMTETCPI 334 Query: 341 HSICEWRREWDSLPLEEQAK-LKARQGIPYVSFEMDVFDANGKPVPWDGKTIGEVVMRGH 399 + +L E + + RQG E+ V +G+ PWDG+T G +++RG Sbjct: 335 GVVATPTPALAALGEEAMDEAIWTRQGRLQFGIELKVETEDGQAAPWDGETSGALLVRGP 394 Query: 400 NVALGYYKNPEKTAESFRDGWFHSGDAAVVHPDGYIEIVDRFKDLINTGGEKVSSILVEK 459 V Y++ A DG+F +GD A + +G++ I DR KD+I +GGE +SSI +E Sbjct: 395 WVVKRYFRKDADAARE--DGFFDTGDIATLDANGFMRITDRQKDVIKSGGEWISSIDLEN 452 Query: 460 TLMEIPGVKAVAVYGTPDEKWGEVVTARIELQEGVKLTEEEVIKFCKERLAHFECPKIVE 519 + PGVK AV G P KW E IE EG ++T+ V+ + R+ + P V Sbjct: 453 VAVGCPGVKIAAVIGVPHPKWEERPLLVIETHEGAEVTKAAVLDYLTPRIVKWWTPDDVV 512 Query: 520 FGPIPMTATGKMQKYVLRNEAK 541 F +P+TATGK+ K VLR K Sbjct: 513 FATVPLTATGKIDKKVLRQAWK 534 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: 700 Number of extensions: 34 Number of successful extensions: 5 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: 549 Length of database: 539 Length adjustment: 35 Effective length of query: 514 Effective length of database: 504 Effective search space: 259056 Effective search space used: 259056 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 Jul 25 2024. The underlying query database was built on Jul 25 2024.
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