Align Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase (EC 2.3.1.168) (characterized)
to candidate 6937555 Sama_1711 dihydrolipoamide acetyltransferase (RefSeq)
Query= reanno::Marino:GFF1672 (378 letters) >FitnessBrowser__SB2B:6937555 Length = 527 Score = 388 bits (996), Expect = e-112 Identities = 213/382 (55%), Positives = 267/382 (69%), Gaps = 12/382 (3%) Query: 1 MTDKAMVEITAPKAGRVTKLYHQQQAMAKVHAPLFAFIPRDREEP--EEARTKPEPAAQL 58 MTDKA+V+I A KAG++ L++++ +AKVHAPL+A I D E P A A Q Sbjct: 152 MTDKALVQIPALKAGKIVTLHYRKGQLAKVHAPLYA-IEVDAEHPVVPPAAAPAAAANQA 210 Query: 59 STATASPVAAASRQRIPASPAVRRLVREHELNLSDIQGSGKDGRVLKADVLAYIEEGPKQ 118 S A + ASPAVRR+ R +++LS + GSGK GRV K D+ Y++ G Sbjct: 211 ERVAPSTAAVNGNGKALASPAVRRMARSLDVDLSLVPGSGKHGRVYKEDIEQYLKGGAAP 270 Query: 119 A---QNQAPADDAQTATTRSARRAPAADQEARVEPIRGIKAAMAKSMVKSATTIPHFIYS 175 A Q AP Q A T+SA PAAD RVEPIRG+KAAMA+ M+ S ++IPHF Y Sbjct: 271 APVAQTAAP----QAAVTQSAPVLPAADD--RVEPIRGVKAAMARQMMDSVSSIPHFTYC 324 Query: 176 EDIDVTDLLKLREQLKPEAEARGSRLTLMPFFMKAMALAVQEFPVLNSQLNDDVTEIHYL 235 E+ID+T+L+ LRE++K + + +LT+MPFFMK+++LA+ EFPV+NSQ+N D TE+ Y Sbjct: 325 EEIDLTELVALRERMKAKYSSDDVKLTMMPFFMKSLSLALTEFPVVNSQVNADCTELTYK 384 Query: 236 PQCNIGMAVDGKAGLTVPNIKGVESLSLLGIADEVARLTEAARSGRVSQEDLKGGTITIS 295 NIGMAVD K GL VPN+K V+S S+L +A E+ RLT+AARSGRVS DLKGGTI+IS Sbjct: 385 ASHNIGMAVDSKVGLLVPNVKDVQSKSILDVAREITRLTDAARSGRVSPADLKGGTISIS 444 Query: 296 NIGALGGTYTAPIINAPEVAIVALGRTQKLPRFDANGQVVERAIMTVSWAGDHRIIDGGT 355 NIGALGGT PIIN PEVAIVALG+ Q LPRF A+G V R IM VSW+GDHR+IDGGT Sbjct: 445 NIGALGGTVATPIINKPEVAIVALGKLQTLPRFGADGSVQARKIMQVSWSGDHRVIDGGT 504 Query: 356 IARFCNRWKGYLESPQTMLLHM 377 IARFCN WK YLE P+ MLL M Sbjct: 505 IARFCNLWKQYLEQPEDMLLAM 526 Score = 56.6 bits (135), Expect = 2e-12 Identities = 34/75 (45%), Positives = 47/75 (62%), Gaps = 4/75 (5%) Query: 1 MTDKAMVEITAPKAGRVTKLYHQQQAMAKVHAPLFAFIPRDREEPEEARTKPEPAAQL-- 58 MTDKA+V+I AP AG V+KLY+ + +AKVHAPL+A + + E + + E AQ Sbjct: 40 MTDKALVQIPAPFAGVVSKLYYAKGEIAKVHAPLYA-VEMEGEGTDASAAPAEANAQAAH 98 Query: 59 -STATASPVAAASRQ 72 S A+PVA A +Q Sbjct: 99 DSVPVAAPVAVAGKQ 113 Lambda K H 0.316 0.131 0.367 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: 532 Number of extensions: 21 Number of successful extensions: 4 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: 378 Length of database: 527 Length adjustment: 32 Effective length of query: 346 Effective length of database: 495 Effective search space: 171270 Effective search space used: 171270 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: 51 (24.3 bits)
This GapMind analysis is from Apr 09 2024. 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