Align methylcrotonoyl-CoA carboxylase (subunit 2/2) (EC 6.4.1.4) (characterized)
to candidate WP_022601566.1 NSB1T_RS24075 acetyl-CoA carboxylase biotin carboxylase subunit
Query= BRENDA::Q9I299 (655 letters) >NCBI__GCF_000473955.1:WP_022601566.1 Length = 503 Score = 453 bits (1165), Expect = e-131 Identities = 233/444 (52%), Positives = 303/444 (68%), Gaps = 1/444 (0%) Query: 8 IQRLLVANRGEIACRVMRSARALGIGSVAVHSDIDRHARHVAEADIAVDLGGAKPADSYL 67 I+++LVANRGEIA RVMRS + + I ++AV S+ DR ARHV AD A +G A+ +SYL Sbjct: 2 IKKILVANRGEIAVRVMRSCKEMEIRTIAVFSEADRAARHVMYADEAYCIGPAEARESYL 61 Query: 68 RGDRIIAAALASGAQAIHPGYGFLSENADFARACEEAGLLFLGPPAAAIDAMGSKSAAKA 127 DRII AL GA AIHPGYGFLSEN DFAR C AG++F+GP ++ MG K +A+ Sbjct: 62 NIDRIIQVALEHGADAIHPGYGFLSENPDFARRCRRAGIVFIGPEPETMEVMGDKISARR 121 Query: 128 LMEEAGVPLVPGYHGEAQDLETFRREAGRIGYPVLLKAAAGGGGKGMKVVEREAELAEAL 187 M EAGVP+VPG E RIGYPV+LKA+AGGGGKGM++ R E+ EA Sbjct: 122 RMREAGVPVVPGTTENLNSSEEAIDVCNRIGYPVMLKASAGGGGKGMRLARRPEEVEEAF 181 Query: 188 SSAQREAKAAFGDARMLVEKYLLKPRHVEIQVFADRHGHCLYLNERDCSIQRRHQKVVEE 247 +A+ EA A+FGD + +EK+++ P H+E Q+ DRHG+ ++L ER+CS+QRR+QK+VEE Sbjct: 182 LAAKSEALASFGDDTVYIEKFVVHPHHIEFQILGDRHGNVIHLCERECSVQRRNQKIVEE 241 Query: 248 APAPGLGAELRRAMGEAAVRAAQAIGYVGAGTVEFLLDERGQFFFMEMNTRLQVEHPVTE 307 P+P + LRR MGE AV AA+A+ YVGAGT+EFL+D G +FF+EMNTRLQVEHP+TE Sbjct: 242 TPSPFISEALRRDMGEKAVAAAKAVNYVGAGTIEFLVDGDGNYFFLEMNTRLQVEHPITE 301 Query: 308 AITGLDLVAWQIRVARGEALPLTQEQVPLNGHAIEVRLYAEDPEGDFLPASGRLMLYREA 367 + G+DLV QI +A G L L Q + GHAIE R+ AED DFLPA G + E Sbjct: 302 EVLGIDLVKEQIHIANGRPLRLRQGDIIQRGHAIECRICAEDTLADFLPAPGIVRQITE- 360 Query: 368 AAGPGRRVDSGVREGDEVSPFYDPMLAKLIAWGETREEARQRLLAMLAETSVGGLRTNLA 427 G G RVDS V EG E+ FYDPM+ KLI W RE A +R+ +L E + G++TN+A Sbjct: 361 PNGIGVRVDSYVYEGYEIPVFYDPMIGKLIVWATCREYAIERMRRVLFEYKITGVKTNIA 420 Query: 428 FLRRILGHPAFAAAELDTGFIARH 451 +LRRI+ P F DTGF+ ++ Sbjct: 421 YLRRIMDTPDFVTGGYDTGFVEKN 444 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: 783 Number of extensions: 17 Number of successful extensions: 2 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: 503 Length adjustment: 36 Effective length of query: 619 Effective length of database: 467 Effective search space: 289073 Effective search space used: 289073 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: 53 (25.0 bits)
This GapMind analysis is from Sep 24 2021. 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