Align Lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex; EC 2.3.1.168; Branched-chain alpha-keto acid dehydrogenase complex component E2; BCKAD-E2; BCKADE2; Dihydrolipoamide acetyltransferase component of branched-chain alpha-keto acid dehydrogenase complex; Dihydrolipoamide branched chain transacylase; Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase (uncharacterized)
to candidate WP_011995836.1 XAUT_RS00790 2-oxoglutarate dehydrogenase complex dihydrolipoyllysine-residue succinyltransferase
Query= curated2:P37942 (424 letters) >NCBI__GCF_000017645.1:WP_011995836.1 Length = 409 Score = 275 bits (703), Expect = 2e-78 Identities = 160/412 (38%), Positives = 227/412 (55%), Gaps = 16/412 (3%) Query: 5 QMTMPQLGESVTEGTISKWLVAPGDKVNKYDPIAEVMTDKVNAEVPSSFTGTITELVGEE 64 ++ +P LGESVTE TI KW PGD V +P+ E+ TDKV EVP+ G + E+V ++ Sbjct: 4 EIRVPTLGESVTEATIGKWFKKPGDTVKADEPLVELETDKVTVEVPAPAAGVLAEIVAKD 63 Query: 65 GQTLQVGEMICKIET-EGANPAEQKQEQPAASEAAENPVAKSAGAADQPNKKRYSPAVLR 123 G T+ VG ++ I GA A PA + AA P A A PAV R Sbjct: 64 GDTVGVGALLGSIGAGSGAAAAAPAAAAPAPAAAAPAPAPAPAAAPAASGSSVNGPAVGR 123 Query: 124 LAGEHGIDLDQVTGTGAGGRITRKDIQRLIETGGVQEQNPEELKTAAPAPKSASKPEPKE 183 +A E G+D V G+G GR+T+ D+ + G AA AP +A P Sbjct: 124 IAAESGVDPSGVAGSGKDGRVTKGDMLAAVAAG------------AAAAPAAA--PIAVR 169 Query: 184 ETSYPASAAGDKEIPVTGVRKAIASNMKRSKTEIPHAWTMMEVDVTNMVAYRNSIKDSFK 243 S P A ++ + +T +R+ IA +K ++ T +VD++ +++ R KD+F+ Sbjct: 170 APSAPIDAVREERVKMTKLRQTIARRLKDAQNTAAMLTTFNDVDMSAVMSLRAQFKDAFE 229 Query: 244 KTEGFNLTFFAFFVKAVAQALKEFPQMNSMWAGDKIIQKKDINISIAVATEDSLFVPVIK 303 K G L F FF KAV ALK+ P +N+ G ++ K NI IAV TE L VPV++ Sbjct: 230 KKHGTKLGFMGFFTKAVIAALKDLPAVNAEIDGQDLVYKNYYNIGIAVGTEKGLVVPVVR 289 Query: 304 NADEKTIKGIAKDITGLAKKVRDGKLTADDMQGGTFTVNNTGSFGSVQSMGIINYPQAAI 363 +AD+ ++ I K I G +K RDGKL +DMQGGTFT+ N G +GS+ S I+N PQ+ I Sbjct: 290 DADQLSVAEIEKAIAGFGRKARDGKLGIEDMQGGTFTITNGGIYGSLMSTPILNAPQSGI 349 Query: 364 LQVESIVKRPVVMDNGMIAVRDMVNLCLSLDHRVLDGLVCGRFLGRVKQILE 415 L + I +RPV + G + +R M+ L LS DHR++DG FL RVK+ LE Sbjct: 350 LGMHRIEERPVAI-KGQVVIRPMMYLALSYDHRIVDGREAVTFLVRVKETLE 400 Lambda K H 0.312 0.129 0.359 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: 414 Number of extensions: 23 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: 424 Length of database: 409 Length adjustment: 31 Effective length of query: 393 Effective length of database: 378 Effective search space: 148554 Effective search space used: 148554 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 42 (21.9 bits) S2: 50 (23.9 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