Align Propionyl-CoA carboxylase, carboxyltransferase subunit; PCC; EC 6.4.1.3 (characterized)
to candidate 351445 BT1917 propionyl-CoA carboxylase beta chain (NCBI ptt file)
Query= SwissProt::I3R7F1 (516 letters) >FitnessBrowser__Btheta:351445 Length = 511 Score = 609 bits (1570), Expect = e-179 Identities = 300/506 (59%), Positives = 384/506 (75%), Gaps = 6/506 (1%) Query: 11 REKREEALKGGGEDRIASQHDKGKMTARERIDYFLDDGTFREFDQFRTHRNHKFGMEETK 70 +E+ A GGG ++I QH+ GKMTARERI+ LD GTF E D+ HR +GM++ K Sbjct: 12 QERDRIASLGGGVEKIEKQHESGKMTARERIEMLLDKGTFVELDKLMVHRCTNYGMDKNK 71 Query: 71 LPGDGVITGHGEVDGRTVFVFAHDFTVFGGSLGEVFAEKICKVMDKAMEVGAPVIGLNDS 130 +PGDG+++G+G++DGR VFV+A+DFTV+GGSL A+KI KV A++ GAP+I LNDS Sbjct: 72 IPGDGIVSGYGKIDGRQVFVYAYDFTVYGGSLSASNAKKIVKVQQLALKNGAPIIALNDS 131 Query: 131 AGARIQEGVQSLGGFGEIFRRNTEASGVVPQISAIMGPCAGGAVYSPALTDFTFMVRDTS 190 GARIQEG++SL G+ +IF +NT ASGV+PQISAI+GPCAGGA YSPALTDF FMV++ S Sbjct: 132 GGARIQEGIESLSGYADIFYQNTMASGVIPQISAILGPCAGGACYSPALTDFIFMVKEKS 191 Query: 191 HMFITGPDVIKTVTGEEVTFDELGGATTHTSTSGVAHFATDTEEQALDDIRHLLSYLPQN 250 HMF+TGPDV+KTV EEV+ +ELGGA TH+S SGV HF +TEE+ L IR LLS+LPQN Sbjct: 192 HMFVTGPDVVKTVIHEEVSKEELGGAMTHSSKSGVTHFMCNTEEELLMSIRELLSFLPQN 251 Query: 251 NVEDPPRVEPWDDPERVADELEEIVPDQPRKPYDIHDVLNGVLDEGSFFGVQEDFAKNIV 310 N+++ + D+ R L+ IVP P PYD+ D++ V+D G FF V +FAKNI+ Sbjct: 252 NMDETKKQNCTDETNREDAVLDTIVPADPNVPYDMKDIIERVVDNGYFFEVMTNFAKNII 311 Query: 311 VGFGRLDGHSVGIVANQPRVNAGTLDIEASEKGARFIRFCDSFNIPILSFVDVPGFLPGT 370 +GF RL G SVGIVANQP AG LDI+AS+K +RFIRFCD FNIP+++F DVPGFLPG Sbjct: 312 IGFARLAGRSVGIVANQPAYLAGVLDIDASDKASRFIRFCDCFNIPLITFEDVPGFLPGY 371 Query: 371 DQEHNGIIRHGAKLLYAYSEATVPLMTVITRKAYGGAYDVMASKHLGADVNYAWPTAEIA 430 QE+NGIIRHGAK++YA++EATVP +TVITRKAYGGAY VM SK GADVN+A+P+AEIA Sbjct: 372 TQENNGIIRHGAKIVYAFAEATVPKLTVITRKAYGGAYIVMNSKQTGADVNFAYPSAEIA 431 Query: 431 VMGPQGAVNILYRDELEAADDPDARRDELIEEYREEFANPYTAADRGFVDDVIEPGDTRN 490 VMG +GAVNIL+R D + + EL E Y+E+FA PY AA+ GF+D++I P TR Sbjct: 432 VMGAEGAVNILFRKA-----DAETKGKEL-EAYKEKFATPYQAAELGFIDEIIYPRQTRK 485 Query: 491 RLIADLRMLKSKRKSQPDKKHGNIPL 516 RLI L M ++K ++ P KKHGN+PL Sbjct: 486 RLIQALEMTENKMQTNPPKKHGNMPL 511 Lambda K H 0.318 0.138 0.407 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: 786 Number of extensions: 28 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: 516 Length of database: 511 Length adjustment: 35 Effective length of query: 481 Effective length of database: 476 Effective search space: 228956 Effective search space used: 228956 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 (21.7 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