Align Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase (EC 2.3.1.168) (characterized)
to candidate Ga0059261_2271 Ga0059261_2271 branched-chain alpha-keto acid dehydrogenase E2 component (EC 2.3.1.168)
Query= reanno::Smeli:SMc03203 (426 letters) >FitnessBrowser__Korea:Ga0059261_2271 Length = 427 Score = 409 bits (1052), Expect = e-119 Identities = 224/430 (52%), Positives = 291/430 (67%), Gaps = 8/430 (1%) Query: 1 MGEFIIKMPDVGEGVAEAELVEWHVKPGDPVREDMVLAAVMTDKATVEIPSPVTGKVLWL 60 M F ++PD+GEG+AEAE+V WHVK GD V ED +A +MTDKATVE+ SPV+G V+ L Sbjct: 1 MARFTFRLPDIGEGIAEAEIVAWHVKVGDRVEEDQQVADMMTDKATVEMESPVSGIVVEL 60 Query: 61 GAEVGDTVAVKAPLVRIETAGEAGEAAPDSIPEALAEQVLDEPVAVSSRLEAKAP-PQPE 119 EVGD VA+ A L+ +ET G+A E+ P++ P A + P AV + +AP P Sbjct: 61 AGEVGDQVAIGAALIVVETDGDAAES-PEAAPALEAVEAPPAPPAVEPPVAPEAPVAPPA 119 Query: 120 KPAPKPAPAPREAPDLSAKP----LASPAVRLRARESGIDLRQVAGTGPAGRITHEDLDL 175 PAP PAPAP A P LASPAVR RA++ GIDL QV RI H DLD Sbjct: 120 PPAPPPAPAPEPVAAAPAAPHRDILASPAVRQRAKDLGIDLSQVKAA-EGDRIRHADLDA 178 Query: 176 FISRGAEPLPAQTGLVRKTAVEEVRMIGLRRRIAEKMSLSTSRIPHITYVEEVDMTALED 235 F+ G+ R V++IG+RR+IAE M+ S IPH TYV+E+D+TALE+ Sbjct: 179 FLRYGSAQGYHAPHASRAREDVPVKVIGMRRKIAENMAASKRAIPHFTYVDEIDVTALEE 238 Query: 236 LRATMNRDRKPEQAKLTILPFLMRALVKTVAEQPGVNATFDDHAGVIHRHAAVHIGIATQ 295 +RA +N +R + KLT+LPF++ A+ +T+ + P +NA +DD AGV+ RH VH+G+ATQ Sbjct: 239 MRADLNANRGA-RPKLTMLPFVIAAICRTLPDFPMLNARYDDEAGVVTRHGRVHMGMATQ 297 Query: 296 TPAGLTVPVVRHAEARGIWDCAAELNRLADAARTGTATRDELTGSTITISSLGAIGGIAS 355 T AGL VPV+R A+ +W AAE+ RLA+AARTG A +EL+GSTITI+SLG +GGIA+ Sbjct: 298 TDAGLMVPVIRDAQDLNVWQLAAEITRLAEAARTGKAKVEELSGSTITITSLGPLGGIAT 357 Query: 356 TPVINHPEVAIVGVNKIAVRPVWDGAQFVPRKIMNLSSSFDHRVIDGWDAAVFVQRLKTL 415 TPVIN PEVAI+G NKI RPV+ G V K+MNLS S DHRV+DGWDAA +VQ L+ L Sbjct: 358 TPVINKPEVAIIGPNKIVERPVFVGDDIVRAKLMNLSISCDHRVVDGWDAASYVQALRKL 417 Query: 416 LETPALIFVE 425 LETP L+F + Sbjct: 418 LETPVLLFAD 427 Lambda K H 0.317 0.133 0.384 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: 527 Number of extensions: 17 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: 426 Length of database: 427 Length adjustment: 32 Effective length of query: 394 Effective length of database: 395 Effective search space: 155630 Effective search space used: 155630 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