Alignments for a candidate for acs in Brucella microti CCM 4915

GapMind for catabolism of small carbon sources

Alignments for a candidate for acs in Brucella microti CCM 4915

Align propionate-CoA ligase (EC 6.2.1.17) (characterized)
to candidate WP_015799731.1 BMI_RS08045 propionyl-CoA synthetase

Query= BRENDA::A0A0G2K047
         (683 letters)



>NCBI__GCF_000022745.1:WP_015799731.1
          Length = 636

 Score =  686 bits (1769), Expect = 0.0
 Identities = 320/626 (51%), Positives = 442/626 (70%), Gaps = 4/626 (0%)

Query: 58  YKTHFAASVADPERFWGKAAEQISWYKPWTKTLENRYPPSTSWFVEGMLNICYNAIDRHI 117
           Y   +AA   DPE FW  AA  I W+KPW +           W+     N CYNA+DRH+
Sbjct: 5   YAETYAAWQNDPEGFWADAAAAIDWFKPWEQVFAGGEGTYGRWYTGAECNTCYNALDRHV 64

Query: 118 ENGQGDKIAIIYDSPVTDTKATISYKEVLEQVSKLAGVLVKQGVKKGDTVVIYMPMIPQA 177
            NG+GD++A+IY+SP+T     I+Y E+LE+V  LA V++  GV+KGD ++IYMP +P+A
Sbjct: 65  ANGRGDQLALIYESPITGKTRKITYHELLEEVEALAAVMLDNGVQKGDRILIYMPTVPEA 124

Query: 178 IYAMLACARIGAIHSLIFGGFASKELSTRIDHVKPKVVVTASFGIEPGRKVEYMPLLEEA 237
           + AMLA ARIGAIHS++FGGFA+ EL+TRID  KP +++ AS GIEP R V Y  +L++A
Sbjct: 125 VVAMLASARIGAIHSVVFGGFAANELATRIDDAKPVMIIAASCGIEPSRVVPYQAMLDKA 184

Query: 238 LRIGQHKPDRLLIYNRPNMEKVPLMSGRDLDWEE--EMAKAQSHDCVPVLSEHPLYILYT 295
           + +  HK D  +I+ R     +P+  GRD+D+ E  + A+ +   CVPV +  PLY+LYT
Sbjct: 185 ISLAHHKVDHCIIFQREQHRHLPV-EGRDIDYREAVDAARGRHVPCVPVAATDPLYVLYT 243

Query: 296 SGTTGLPKGVVRPTGGYAVMLNWTMSSIYGLKPGEVWWAASDLGWVVGHSYICYGPLLHG 355
           SGTTG PKGVVR  GG+ V L W+M  ++ +KPG+VWWAASD+GWVVGHSYI Y PLL G
Sbjct: 244 SGTTGEPKGVVRDNGGHMVALVWSMKHVFDVKPGQVWWAASDVGWVVGHSYIVYAPLLIG 303

Query: 356 NTTVLYEGKPVGTPDAGAYFRVLAEHGVAALFTAPTAIRAIRQQDPGAALGKQYSLTRFK 415
            T++L+EGKPVGTPDAG Y+R++ EHGV  +FTAPTA+RAI+++D      +++ L+ F+
Sbjct: 304 ATSILFEGKPVGTPDAGEYWRIIEEHGVEVMFTAPTALRAIKKEDADGHFVRRHDLSGFR 363

Query: 416 TLFVAGERCDVETLEWSKKVFRVPVLDHWWQTETGSPITASCIGLGNSKTPPPGQAGKCV 475
            L++AGER D ET+ W++ +   PV+DHWWQTE+G P+ A+ +GLG  +T   G    C+
Sbjct: 364 ALYLAGERADPETIHWAENLLGCPVIDHWWQTESGWPMVANPLGLGLLET-KYGSPAVCL 422

Query: 476 PGYNVMILDDNMQKLKARSLGNIVVKLPLPPGAFSGLWKNQEAFKHLYFEKFPGYYDTMD 535
           PGY++ +LDD   +++  +LGNI++KLPLPPG    LW   E F+  Y  +FPGYY T D
Sbjct: 423 PGYDIRVLDDEGHEVEPGTLGNILIKLPLPPGCLPTLWNADERFRKAYLNEFPGYYKTAD 482

Query: 536 AGYMDEEGYLYVMSRVDDVINVAGHRISAGAIEESVLSHGTVTDCAVVGKEDPLKGHVPL 595
           AGYMDE+GYLY+MSR DD+INVAGHR+S GA+EE + SH  V +CAV+G  DPLKG VP 
Sbjct: 483 AGYMDEDGYLYIMSRTDDIINVAGHRLSTGAMEEVLSSHPDVAECAVLGISDPLKGQVPC 542

Query: 596 ALCVLKKDVNATEEQVLEEIVKHVRQSIGPVAAFRNAVFVKQLPKTRSGKIPRSTLSALV 655
              VLK +++   ++V +E +  +R +IGPVAAFR A+ VK+LPKTRSGKI RST+  + 
Sbjct: 543 GFLVLKSNIDRDPQEVEKECISMIRDAIGPVAAFRLALAVKRLPKTRSGKILRSTIQKMA 602

Query: 656 NGKPYKVTPTIEDPSIFGHIEEVLKQ 681
           +G+ +K+  TI+DP+I   I  VL++
Sbjct: 603 DGQEWKMPATIDDPAILDEIGTVLRE 628


Lambda     K      H
   0.318    0.136    0.421 

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: 1324
Number of extensions: 64
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: 683
Length of database: 636
Length adjustment: 38
Effective length of query: 645
Effective length of database: 598
Effective search space:   385710
Effective search space used:   385710
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: 54 (25.4 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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

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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 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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