Align methylcrotonoyl-CoA carboxylase (subunit 2/2) (EC 6.4.1.4) (characterized)
to candidate 6939098 Sama_3196 acetyl-CoA carboxylase, biotin carboxylase (RefSeq)
Query= BRENDA::Q9I299 (655 letters) >FitnessBrowser__SB2B:6939098 Length = 454 Score = 364 bits (934), Expect = e-105 Identities = 212/458 (46%), Positives = 278/458 (60%), Gaps = 13/458 (2%) Query: 3 PDYRSIQRLLVANRGEIACRVMRSARALGIGSVAVHSDIDRHARHVAEADIAVDLGGAKP 62 P +R+LVANRGEIA R++R+ LG+ +VA++S D+ A H A + +G A Sbjct: 2 PTEARFKRVLVANRGEIAVRIIRACHQLGLETVAIYSSADKGALHTLLATHCLCIGPAAA 61 Query: 63 ADSYLRGDRIIAAALASGAQAIHPGYGFLSENADFARACEEAGLLFLGPPAAAIDAMGSK 122 DSYL + I+ AA + A AIHPGYGFL+E A FARA EAGL+FLGP A I MG K Sbjct: 62 KDSYLNINAILEAAKLTAADAIHPGYGFLAERAGFARAVTEAGLVFLGPDADTIATMGDK 121 Query: 123 SAAKALMEEAGVPLVPGYHGEA-QDLETFRREAGRIGYPVLLKAAAGGGGKGMKVVEREA 181 +A ++ G+P +PG G D+ A IGYPVL+KA+AGGGG+GM+ V+ Sbjct: 122 VSAIKSIKAVGIPTLPGSDGALNDDMNAVEALATDIGYPVLIKASAGGGGRGMRRVDSAD 181 Query: 182 ELAEALSSAQREAKAAFGDARMLVEKYLLKPRHVEIQVFADRHGHCLYLNERDCSIQRRH 241 ELA A++ + EA AAFGD + +EK+L PRH+E Q+ AD L L ERDCS QRRH Sbjct: 182 ELASAIALTRSEALAAFGDNTVYLEKFLTHPRHIEFQMLADGEA-ALCLGERDCSAQRRH 240 Query: 242 QKVVEEAPAPGLGAELRRAMGEAAVRAAQAIGYVGAGTVEFLLDERGQFFFMEMNTRLQV 301 QK++EEAPA G+ E R M + A + +GY G GT EFL + G FFF+EMNTR+QV Sbjct: 241 QKLIEEAPALGIAREKIREMADICEAACRRLGYRGVGTFEFLYQD-GAFFFIEMNTRIQV 299 Query: 302 EHPVTEAITGLDLVAWQIRVARGEALPLTQEQVPLNGHAIEVRLYAEDPEGDFLPASGRL 361 EH VTE +TGLDL+AWQ++VA G LP + + GHAIE R+ AE P+ LP+ G + Sbjct: 300 EHTVTEMVTGLDLIAWQLKVALGHPLP---PRPQVQGHAIECRINAEAPQSQ-LPSPGVI 355 Query: 362 MLYREAAAGPGRRVDSGVREGDEVSPFYDPMLAKLIAWGETREEARQRLLAMLAETSVGG 421 R GPG R DS + G V FYD ++ KLI G TREEA RL L E + G Sbjct: 356 TQLR-VPGGPGVRWDSYLFPGAMVPAFYDSLIGKLICHGVTREEATARLRQALTELEIQG 414 Query: 422 LRTNLAFLRRILGHPAFAAAELDTGFIARHQDDLLPAP 459 + N + +++ AF + D F+ D L AP Sbjct: 415 IAINKSLHLQLIACDAFQPWQRDIHFV-----DALSAP 447 Lambda K H 0.319 0.135 0.397 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: 699 Number of extensions: 33 Number of successful extensions: 6 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: 655 Length of database: 454 Length adjustment: 35 Effective length of query: 620 Effective length of database: 419 Effective search space: 259780 Effective search space used: 259780 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: 52 (24.6 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