Aligments for a candidate for pccA1 in Shewanella oneidensis MR-1

GapMind for catabolism of small carbon sources

Aligments for a candidate for pccA1 in Shewanella oneidensis MR-1

Align acyl CoA carboxylase biotin carboxylase subunit (EC 2.1.3.15; EC 6.4.1.3; EC 6.3.4.14) (characterized)
to candidate 201056 SO1894 acetyl-CoA carboxylase, biotin carboxylase, putative (NCBI ptt file)

Query= metacyc::MONOMER-13597
         (509 letters)



>FitnessBrowser__MR1:201056
          Length = 694

 Score =  373 bits (958), Expect = e-107
 Identities = 205/493 (41%), Positives = 290/493 (58%), Gaps = 6/493 (1%)

Query: 4   FSRVLVANRGEIATRVLKAIKEMGMTAIAVYSEADKYAVHTKYADEAYYIGKAPALDSYL 63
           F+++L+ANRGEIA R++K  + MG+  +A+YS+ADK A H   ADE++Y+G +   DSYL
Sbjct: 12  FTKLLIANRGEIACRIIKTAQAMGVRTVALYSDADKNARHVAMADESFYLGGSAPADSYL 71

Query: 64  NIEHIIDAAEKAHVDAIHPGYGFLSENAEFAEAVEKAGITFIGPSSEVMRKIKDKLDGKR 123
             + II  A+KA   AIHPGYGFLSENA+FA   E AGI F+GP S+ +  +  K   K 
Sbjct: 72  KGDLIIAIAKKAQAQAIHPGYGFLSENADFARKCEAAGIVFVGPGSDAIDAMGSKSAAKA 131

Query: 124 LANMAGVPTAPGSDGPVTSIDEALKL-AEKIGYPIMVKAASGGGGVGITRVDNQDQLMDV 182
           +   A VP  PG  G     D  LK  A KIG+P+++KAA GGGG G+  V+++ ++MD 
Sbjct: 132 IMTAAQVPLVPGYHGD-DQTDATLKAEALKIGFPMLIKAAYGGGGKGMRIVEHEGEIMDA 190

Query: 183 WERNKRLAYQAFGKADLFIEKYAVNPRHIEFQLIGDKYGNYVVAWERECTIQRRNQKLIE 242
               +R A  +FG   L +E+Y   PRH+E Q+  D +GN +   +R+C+IQRR+QK++E
Sbjct: 191 INSARREAASSFGNDKLLMERYLRQPRHVEVQVFADTFGNAIYLSDRDCSIQRRHQKVVE 250

Query: 243 EAPSPALKMEERESMFEPIIKFGKLINYFTLGTFETAFSDVSRDFYFLELNKRLQVEHPT 302
           EAP+P L  E R  M E  +   K I+Y   GT E    D    FYF+E+N RLQVEHP 
Sbjct: 251 EAPAPGLSDELRAQMGEAAVAAAKAIDYVGAGTIEFLL-DTDNSFYFMEMNTRLQVEHPV 309

Query: 303 TELIFRIDLVKLQIKLAAGEHLPFSQEDLNKRVRGTAIEYRINAEDALNNFTGSSGFVTY 362
           TE++   DLVK Q+ +A+G+ LP  Q+++  R+ G A E RI AED  N F  +SG + +
Sbjct: 310 TEMVTGQDLVKWQLMVASGQPLPLKQDEV--RIHGHAFEVRIYAEDPQNEFLPASGKLNF 367

Query: 363 YREP-TGPGVRVDSGIESGSYVPPYYDSLVSKLIVYGESREYAIQAGIRALADYKIGGIK 421
            REP     VR+DSGI     +  +YD +++KLIV+ ESR  A+Q  + AL  Y+I G+K
Sbjct: 368 LREPEQSKYVRIDSGIRENDVISNFYDPMIAKLIVWDESRPRALQRLVHALESYQISGLK 427

Query: 422 TTIELYKWIMQDPDFQEGKFSTSYISQKTDQFVKYLREQEEIKAAIAAEIQSRGLLRTSS 481
             IE    I + P F +  FST +I++  D  +     + +   A AA  Q       + 
Sbjct: 428 HNIEFLANIAEHPAFAKADFSTDFINRYGDALIGSASSEADTALAFAALYQVLARKEAAK 487

Query: 482 TDNKGKAQSKSGW 494
                 A   S W
Sbjct: 488 AQAINSADPDSPW 500


Lambda     K      H
   0.317    0.135    0.385 

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: 774
Number of extensions: 37
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: 509
Length of database: 694
Length adjustment: 37
Effective length of query: 472
Effective length of database: 657
Effective search space:   310104
Effective search space used:   310104
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: 53 (25.0 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

Related tools

About GapMind

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources