Aligments for a candidate for ackA in Desulfovibrio vulgaris Miyazaki F

GapMind for catabolism of small carbon sources

Aligments for a candidate for ackA in Desulfovibrio vulgaris Miyazaki F

Align Formate-dependent phosphoribosylglycinamide formyltransferase; 5'-phosphoribosylglycinamide transformylase 2; Formate-dependent GAR transformylase; GAR transformylase 2; GART 2; Non-folate glycinamide ribonucleotide transformylase; Phosphoribosylglycinamide formyltransferase 2; EC 2.1.2.- (characterized)
to candidate 8502043 DvMF_2756 phosphoribosylglycinamide formyltransferase 2 (RefSeq)

Query= SwissProt::P33221
         (392 letters)



>FitnessBrowser__Miya:8502043
          Length = 393

 Score =  492 bits (1266), Expect = e-144
 Identities = 248/392 (63%), Positives = 307/392 (78%), Gaps = 1/392 (0%)

Query: 1   MTLLGTALRPAATRVMLLGSGELGKEVAIECQRLGVEVIAVDRYADAPAMHVAHRSHVIN 60
           M  +GT   P+ATR++LLGSGELG+EVAIE  RLGVEVIAVDRY +APAM VAHRSHV++
Sbjct: 1   MVTIGTPNTPSATRILLLGSGELGREVAIEAMRLGVEVIAVDRYPNAPAMQVAHRSHVVS 60

Query: 61  MLDGDALRRVVELEKPHYIVPEIEAIATDMLIQLEEEGLNVVPCARATKLTMNREGIRRL 120
           MLDG ALRR++E E+PH IVPEIEAIAT+ L++LE+EG  VVP ARA +LTM+REGIRRL
Sbjct: 61  MLDGAALRRIIEAERPHCIVPEIEAIATETLLELEKEGFRVVPTARAARLTMDREGIRRL 120

Query: 121 AAEELQLPTSTYRFADSESLFREAVADIGYPCIVKPVMSSSGKGQTFIRSAEQLAQAWKY 180
           AAEEL LPTS YRFA++E+ +REAVA +G PC+VKPVMSSSGKGQ+ +R+   + +AW+Y
Sbjct: 121 AAEELGLPTSPYRFAETEAEYREAVAAVGLPCVVKPVMSSSGKGQSTVRTEADVMKAWEY 180

Query: 181 AQQGGRAGAGRVIVEGVVKFDFEITLLTVSAVDGVHFCAPVGHRQEDGDYRESWQPQQMS 240
           AQ GGRAG G+VIVEG V FD+EIT LTV    G  FC P+GH Q+DGDYRESWQP  MS
Sbjct: 181 AQTGGRAGGGKVIVEGFVDFDYEITQLTVRHAGGTTFCDPIGHLQKDGDYRESWQPHPMS 240

Query: 241 PLALERAQEIARKVVLALGGYGLFGVELFVCGDEVIFSEVSPRPHDTGMVTLISQDLSEF 300
             AL  ++ +A  V  ALGG+G+FGVELF+ GD+V FSEVSPRPHDTG+VTLISQ+LSEF
Sbjct: 241 QAALAESRRMAEAVTGALGGWGIFGVELFIKGDKVYFSEVSPRPHDTGLVTLISQNLSEF 300

Query: 301 ALHVRAFLGLPVGGIRQYGPAASAVILPQLTSQNVTFDNVQNAVG-ADLQIRLFGKPEID 359
           ALH RA LGLPV  +RQ GPAAS V+L +  S +  +  ++ A+   D  + LFGKPE+ 
Sbjct: 301 ALHARAILGLPVPALRQNGPAASCVVLAEGDSMSPGYHGIEAALAEPDTGLCLFGKPEVH 360

Query: 360 GSRRLGVALATAESVVDAIERAKHAAGQVKVQ 391
           G RR+GVALA   S+ +A  +A+ AA  V+V+
Sbjct: 361 GKRRMGVALALGASIEEARAKARRAAAAVQVE 392


Lambda     K      H
   0.320    0.136    0.390 

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: 468
Number of extensions: 16
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: 392
Length of database: 393
Length adjustment: 31
Effective length of query: 361
Effective length of database: 362
Effective search space:   130682
Effective search space used:   130682
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: 50 (23.9 bits)

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

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Protein sequences (fasta format)
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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, 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