Aligments for a candidate for pgmA in Pseudomonas fluorescens GW456-L13

GapMind for catabolism of small carbon sources

Aligments for a candidate for pgmA in Pseudomonas fluorescens GW456-L13

Align phosphomannomutase (EC 5.4.2.8) (characterized)
to candidate PfGW456L13_794 Phosphomannomutase (EC 5.4.2.8) / Phosphoglucomutase (EC 5.4.2.2)

Query= BRENDA::P26276
         (463 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_794
          Length = 465

 Score =  723 bits (1866), Expect = 0.0
 Identities = 356/459 (77%), Positives = 404/459 (88%), Gaps = 2/459 (0%)

Query: 6   APTLPASIFRAYDIRGVVGDTLTAETAYWIGRAIGSESLARGEPCVAVGRDGRLSGPELV 65
           AP  P SIFRAYDIRG V + L AETAYWIGRA+GS+SLA+GEP V+VGRDGRLSGPELV
Sbjct: 8   APKFPDSIFRAYDIRGTVPEFLNAETAYWIGRAVGSQSLAQGEPNVSVGRDGRLSGPELV 67

Query: 66  KQLIQGLVDCGCQVSDVGMVPTPVLYYAANVLEGKSGVMLTGSHNPPDYNGFKIVVAGET 125
            QLI+G+ D GC VSDVG+VPTP LYYAANVL GKSGVMLTGSHNP +YNGFKIV+AG+T
Sbjct: 68  AQLIKGIADSGCHVSDVGLVPTPALYYAANVLAGKSGVMLTGSHNPSNYNGFKIVIAGDT 127

Query: 126 LANEQIQALRERIEKNDLASGVGSVEQVDILPRYFKQIRDDIAMAKPMKVVVDCGNGVAG 185
           LANEQIQAL +R++ N+L+SG GS+ QV+IL RY  +I  DI +A+ +KVVVDCGNG AG
Sbjct: 128 LANEQIQALHDRLKTNNLSSGQGSITQVEILDRYTTEIVQDIKLARRLKVVVDCGNGAAG 187

Query: 186 VIAPQLIEALGCSVIPLYCEVDGNFPNHHPDPGKPENLKDLIAKVKAENADLGLAFDGDG 245
           VIAPQLIEAL C VIPL+CEVDGNFPNHHPDPGKPENL DLIAKVK  NAD+GLAFDGDG
Sbjct: 188 VIAPQLIEALNCEVIPLFCEVDGNFPNHHPDPGKPENLVDLIAKVKETNADIGLAFDGDG 247

Query: 246 DRVGVVTNTGTIIYPDRLLMLFAKDVVSRNPGADIIFDVKCTRRLIALISGYGGRPVMWK 305
           DRVGVVTNTG+I+YPDRLLMLFA+DVV+RNPGA+IIFDVKCTRRLI LI  YGGR +MWK
Sbjct: 248 DRVGVVTNTGSIVYPDRLLMLFARDVVARNPGAEIIFDVKCTRRLIPLIKEYGGRSLMWK 307

Query: 306 TGHSLIKKKMKETGALLAGEMSGHVFFKERWFGFDDGIYSAARLLEILSQDQRDSEHVFS 365
           TGHSLIKKKMK++GALLAGEMSGH+FFKERWFGFDDGIYSAARLLEILS+++  +E +F+
Sbjct: 308 TGHSLIKKKMKQSGALLAGEMSGHIFFKERWFGFDDGIYSAARLLEILSKEKSSAEELFA 367

Query: 366 AFPSDISTPEINITVTEDSKFAIIEALQRDAQWGEG-NITTLDGVRVDYPKGWGLVRASN 424
            FP+DISTPEINI VTE+SKF+II+AL  DAQWGEG ++TT+DGVRVDY KGWGLVRASN
Sbjct: 368 TFPNDISTPEINIHVTEESKFSIIDAL-HDAQWGEGADLTTIDGVRVDYAKGWGLVRASN 426

Query: 425 TTPVLVLRFEADTEEELERIKTVFRNQLKAVDSSLPVPF 463
           TTPVLVLRFEAD E EL+RIK VF  QLK V   L +PF
Sbjct: 427 TTPVLVLRFEADDEAELQRIKDVFHAQLKRVAPDLQLPF 465


Lambda     K      H
   0.319    0.138    0.410 

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: 697
Number of extensions: 20
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: 463
Length of database: 465
Length adjustment: 33
Effective length of query: 430
Effective length of database: 432
Effective search space:   185760
Effective search space used:   185760
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 (21.7 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Sep 17 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 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