Align Acetoacetate--CoA ligase (EC 6.2.1.16) (characterized)
to candidate WP_059150936.1 V474_RS07610 acyl--CoA ligase
Query= reanno::acidovorax_3H11:Ac3H11_3009 (578 letters) >NCBI__GCF_001046635.1:WP_059150936.1 Length = 545 Score = 234 bits (597), Expect = 7e-66 Identities = 171/549 (31%), Positives = 262/549 (47%), Gaps = 23/549 (4%) Query: 30 TIGAFFADMVARQPEREALVSVHQGRRYTYAQLQTEAHRLASALLGMGLTPGDRVGIWSH 89 T+G R +R+A+V RR YA L +A A AL MG+ PGD VG+ Sbjct: 9 TMGEMIRSSGQRFADRDAIV--FPDRRLGYADLNRKARDWARALAAMGVKPGDNVGLLLP 66 Query: 90 NNAEWVLMQLATAQVGLVLVNINPAYRTAEVEYALNKVGCKLLVSMARFKTS-DYLGMLR 148 +++ G V V +N Y+ +E+ + + +++ + D+ L Sbjct: 67 TCLDFITAFYGITMTGAVAVPVNARYQASELGFVVADADLVAIITTGKVADGLDFSARLE 126 Query: 149 ELAPEW-QGQQPGHLQAAKLPQLKTVVWIDDEAGQGADEPGLLRFTELIARG-----NAA 202 P Q P L + P+L+++V +D+ P L+ +A+G + Sbjct: 127 AAMPSLTQSGDPWALSLPEAPRLRSIVCLDERCA-----PYLVPANAALAKGAKIAEDEI 181 Query: 203 DPRLAQVAAGLQATDPINIQFTSGTTGFPKGATLTHRNILNNGFFIGECMKLTPADRLCI 262 D R+ VA D I +TSGTT PKGA ++HR + N +G + T D++ Sbjct: 182 DARIDAVAP----QDTAMILYTSGTTANPKGAMISHRAQVANSRGLGVRYECTEEDKVWS 237 Query: 263 PVPLYHCFGMVLGNLACFTHGATIVYPNDGFDPLTVLQTVQDERCTGLHGVPTMFIAEL- 321 P+P++H G++ + G + P FD L+ + E T + + +L Sbjct: 238 PLPIFHIAGILPMTMILDIGGVYMTIPR--FDAGVGLEMLGREGATIAYPSFVTIMQDLI 295 Query: 322 DHPRFAEFNLSTLRTGIMAGSPCPTEVMKRVVEQMNLREITIAYGMTETSPVSCQSSTDT 381 HP F + +LS LR + P + V E M YG+TE + S Sbjct: 296 THPTFKDTDLSRLRIMNSNFAVQPEWIKLAVAEAMPHTIQVGTYGLTEGAGTVSTSRLSD 355 Query: 382 PLSKRVSTVGQVQPHLEVKIVDPDTGAVVPIGQRGEFCTKGYSVMHGYWGDEAKTREAID 441 R G +V+IVDP+TGA G+ GE G +V+ GY+ KT EAI Sbjct: 356 SYEVRTGRCGVPLEEWQVRIVDPETGADCGPGEHGEIVLGGPNVLKGYYNAPEKTAEAIR 415 Query: 442 EGGWMHTGDLATMDAEGYVNIVGRIKDMVIRGGENIYPREIEEFLYRHPQVQDVQVVGVP 501 +G W +GD+ ++DA G V GR KDM+ GGEN+ EIE L HP V+ QVVG+P Sbjct: 416 DG-WFFSGDIGSIDANGNVMFHGRTKDMLKVGGENVAAAEIEAMLQTHPAVKLAQVVGLP 474 Query: 502 DQKYGEELCAWIIAKPGTQPTEDDIRAFCKGQIAHYKVPRYIRFVTSFPMTVTGKIQKFK 561 D +Y E A++ G +E ++ CKG+IA +KVPR+IRFV +PM+ T KIQKF+ Sbjct: 475 DDRYAEVPAAFVELAEGAAASEQELIDHCKGRIAGFKVPRHIRFVEEWPMS-TSKIQKFR 533 Query: 562 IRDEMKDQL 570 +R+ + +L Sbjct: 534 LREGLIAEL 542 Lambda K H 0.320 0.136 0.412 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: 727 Number of extensions: 33 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: 578 Length of database: 545 Length adjustment: 36 Effective length of query: 542 Effective length of database: 509 Effective search space: 275878 Effective search space used: 275878 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 (21.8 bits) S2: 53 (25.0 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