Alignments for a candidate for acs in Mesorhizobium ciceri WSM1271

GapMind for catabolism of small carbon sources

Alignments for a candidate for acs in Mesorhizobium ciceri WSM1271

Align propionate-CoA ligase (EC 6.2.1.17) (characterized)
to candidate YP_004139446.1 Mesci_0223 AMP-dependent synthetase and ligase

Query= BRENDA::A0A0G2K047
         (683 letters)



>NCBI__GCF_000185905.1:YP_004139446.1
          Length = 635

 Score =  672 bits (1735), Expect = 0.0
 Identities = 321/618 (51%), Positives = 431/618 (69%), Gaps = 6/618 (0%)

Query: 68  DPERFWGKAAEQISWYKPWTKTLENRYPPSTSWFVEGMLNICYNAIDRHIENGQGDKIAI 127
           DPE+FW  AA  I WY PW K  +        WF     N CYNA+DRH+  G+ D+IA+
Sbjct: 15  DPEQFWADAAGAIDWYSPWDKVFDANAGVYGRWFTGATCNTCYNALDRHVAGGRADQIAL 74

Query: 128 IYDSPVTDTKATISYKEVLEQVSKLAGVLVKQGVKKGDTVVIYMPMIPQAIYAMLACARI 187
           I+DS +  T    +Y E+  +V  L  VL  +G++KGD V+IYMPM+ +A  AMLACARI
Sbjct: 75  IHDSAIAGTVKKFTYAELKREVVALTSVLKNRGIRKGDRVIIYMPMVAEAAIAMLACARI 134

Query: 188 GAIHSLIFGGFASKELSTRIDHVKPKVVVTASFGIEPGRKVEYMPLLEEALRIGQHKPDR 247
           GA+HS++FGGFAS EL+TRID  +PK++++AS G+EPGR V Y PLL++A+ I +HKPD 
Sbjct: 135 GAVHSVVFGGFASHELATRIDDARPKLIISASCGLEPGRVVAYKPLLDKAIEISRHKPDA 194

Query: 248 LLIYNRPNMEKVPLMSGRDLDWEEEMAKAQSH----DCVPVLSEHPLYILYTSGTTGLPK 303
            LI  R  + +  L    D+D+ + +A+ ++     DCVPVL+  PLYI+YTSGTTG PK
Sbjct: 195 CLILQRDQL-RCELKEHFDIDYADAVARERAAGANVDCVPVLATDPLYIIYTSGTTGQPK 253

Query: 304 GVVRPTGGYAVMLNWTMSSIYGLKPGEVWWAASDLGWVVGHSYICYGPLLHGNTTVLYEG 363
           G+VR  GG+ V L WTM + +G+KPGEV+WAASD+GWVVGHSYI YGPLLHG T++L+EG
Sbjct: 254 GIVRDNGGHMVALKWTMENEFGVKPGEVFWAASDVGWVVGHSYIVYGPLLHGCTSILFEG 313

Query: 364 KPVGTPDAGAYFRVLAEHGVAALFTAPTAIRAIRQQDPGAALGKQYSLTRFKTLFVAGER 423
           KPVGTPDAG Y+RV+AEHGV ALFTAPTA RAI+ QDP      ++ L++F+TLF+AGER
Sbjct: 314 KPVGTPDAGTYWRVIAEHGVVALFTAPTAFRAIKGQDPKGEFIAKHDLSKFRTLFLAGER 373

Query: 424 CDVETLEWSKKVFRVPVLDHWWQTETGSPITASCIGLGNSKTPPPGQAGKCVPGYNVMIL 483
            D ET++W+++   VPV+DHWWQTETGSP+T +  GLG       G  G  +PGY++ +L
Sbjct: 374 ADPETIKWAEQKLNVPVVDHWWQTETGSPMTINPAGLGLLPV-KYGSPGVPMPGYDIRVL 432

Query: 484 DDNMQKLKARSLGNIVVKLPLPPGAFSGLWKNQEAFKHLYFEKFPGYYDTMDAGYMDEEG 543
           DD   +++  +LGN+V+KLPLP G    LW   + F+  Y ++FPG+Y T DAG +DE+G
Sbjct: 433 DDAGHEVQRGTLGNVVIKLPLPAGCLPTLWNADQRFRQAYLDEFPGFYKTADAGMVDEDG 492

Query: 544 YLYVMSRVDDVINVAGHRISAGAIEESVLSHGTVTDCAVVGKEDPLKGHVPLALCVLKKD 603
           YLYVM+R DD+INVAGHR+S GA+EE + +H  V +CAV+G  D +KG VPL   VL   
Sbjct: 493 YLYVMARTDDIINVAGHRLSTGAMEEVLSAHPDVAECAVIGIADAMKGQVPLGFVVLNAG 552

Query: 604 VNATEEQVLEEIVKHVRQSIGPVAAFRNAVFVKQLPKTRSGKIPRSTLSALVNGKPYKVT 663
           V      +  E+V  VR+ IGPVAAF+  V +K+LPKTRSGKI R T+  + + + + + 
Sbjct: 553 VTRDIGSIENEVVGLVRERIGPVAAFKTVVTIKRLPKTRSGKILRGTMQKIADKEEWAMP 612

Query: 664 PTIEDPSIFGHIEEVLKQ 681
            TI+DP I   I   LK+
Sbjct: 613 ATIDDPVILDEITAALKE 630


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: 1294
Number of extensions: 59
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: 635
Length adjustment: 38
Effective length of query: 645
Effective length of database: 597
Effective search space:   385065
Effective search space used:   385065
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)
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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 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