Align Methylcrotonoyl-CoA carboxylase (EC 6.4.1.4) (characterized)
to candidate WP_013461228.1 SULKU_RS11930 acetyl-CoA carboxylase biotin carboxylase subunit
Query= reanno::pseudo5_N2C3_1:AO356_01595 (649 letters) >NCBI__GCF_000183725.1:WP_013461228.1 Length = 446 Score = 408 bits (1048), Expect = e-118 Identities = 213/444 (47%), Positives = 292/444 (65%), Gaps = 3/444 (0%) Query: 6 LTTLLVANRGEIACRVMRTARAMGLTTVAVHSATDRDARHSREADIRVDLGGSKAADSYL 65 L +LVANRGEIA R +RT + MG VAV+S D+DA + + AD + +G + ++ SYL Sbjct: 4 LKRILVANRGEIALRAIRTIKEMGKEAVAVYSTADKDASYLKLADAAICIGAAPSSQSYL 63 Query: 66 QIDKLIAAAKASGAQAIHPGYGFLSENAGFARAIENAGLIFLGPPASAIDAMGSKSAAKT 125 I +IAA + SG A+ PGYGFLSEN F + G+ F+GP + M KS AK Sbjct: 64 NIPAIIAACEISGCDAVFPGYGFLSENQHFVEICTHHGIKFIGPTPEVMVMMSDKSKAKD 123 Query: 126 LMETAGVPLVPGYHGEAQDLETFRDAAERIGYPVLLKATAGGGGKGMKVVEDVSQLAEAL 185 +M AGVP+VPG G +D+ + A+ +GYPV+LKA AGGGG+GM+VVED S + A Sbjct: 124 VMIAAGVPVVPGSDGAIKDIAEAKVRAKEVGYPVILKAAAGGGGRGMRVVEDESYIENAF 183 Query: 186 ASAQREAQSSFGDSRMLVEKYLLKPRHVEIQVFADQHGNCLYLNERDCSIQRRHQKVVEE 245 +A+ EA +FGD + +EK++ PRH+E+QV AD HGN L++ ERDCS+QRRHQK++EE Sbjct: 184 LAAEAEAIGAFGDGTIYMEKFIKNPRHIEVQVIADSHGNVLHIGERDCSMQRRHQKLIEE 243 Query: 246 APAPGLTPQLRRAMGEAAVRAAQAIGYVGAGTVEFLLDARGEFFFMEMNTRLQVEHPVTE 305 +PA LTP++R + +AVRA + I Y GAGT E+LLDA +F+FMEMNTRLQVEH V+E Sbjct: 244 SPAVALTPEIRAELHASAVRATKYIKYEGAGTFEYLLDADKKFYFMEMNTRLQVEHCVSE 303 Query: 306 AITGLDLVAWQIRVAQGEPLPITQAQVPLLGHAIEVRLYAEDPGNDFLPATGRLALYRES 365 ++GLDL+ IRVA+GE LP +Q V L GH+IE R+ AEDP FLP+ G++ + + Sbjct: 304 MVSGLDLIEMMIRVAEGEALP-SQESVVLKGHSIECRITAEDP-IKFLPSPGKITQW-IA 360 Query: 366 AEGPGRRVDSGVEEGDEISPFYDPMLGKLIAWGEDREQARLRLLSMLDEFVIGGLKTNIG 425 G R+D+ G + P YD M+GKLI +G DR A R+ L EF I G+KT I Sbjct: 361 PGGRNVRIDTHAHAGYIVPPTYDSMIGKLIVYGTDRNDAIARMHRALSEFTITGIKTTIP 420 Query: 426 FLRRIVAHPAFAAAELDTGFIPRY 449 F +++ +P F DT ++ Y Sbjct: 421 FHMKMMKNPDFINNNFDTKYLENY 444 Lambda K H 0.319 0.134 0.390 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: 686 Number of extensions: 27 Number of successful extensions: 3 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: 649 Length of database: 446 Length adjustment: 35 Effective length of query: 614 Effective length of database: 411 Effective search space: 252354 Effective search space used: 252354 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 (21.7 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