GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manA in Sinorhizobium meliloti 1021

Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13) (characterized)
to candidate SM_b21082 SM_b21082 mannose-6-phosphate isomerase, GDP-mannose pyrophosphorylase

Query= BRENDA::P07874
         (481 letters)



>FitnessBrowser__Smeli:SM_b21082
          Length = 767

 Score =  258 bits (660), Expect = 4e-73
 Identities = 144/366 (39%), Positives = 209/366 (57%), Gaps = 13/366 (3%)

Query: 5   ILSGGSGSRLWPLSRKQYPKQFLALTGDDTLFQQTIKRL-AFDGMQAPL-LVCNKEHRFI 62
           ++SGG GSRLWPLSR+  PKQF  L G  ++   T++RL A      P+ ++ ++ H   
Sbjct: 9   VMSGGVGSRLWPLSREDNPKQFHDLAGHGSMLVNTVRRLKARPAGDTPVHVIASERHSER 68

Query: 63  VQEQLEAQNLASQAILLEPFGRNTAPAVAIAAMKLVAEGRDELLLILPADHVIEDQRAFQ 122
           V+  L   +LA    + EP GRNTA AVA+AA++ +A   D L+L++P+DH I  +  F 
Sbjct: 69  VRADLAGIDLAGGHAIFEPVGRNTAAAVAVAALETIATHGDGLVLVVPSDHEISTEEQFW 128

Query: 123 QALALATNAAEKGEMVLFGIPASRPETGYGYIRASADAQLPEGVSRVQSFVEKPDEARAR 182
             +     AAE G +V+FGIP   PETGYGYI +     + +    V  FVEKP    A+
Sbjct: 129 NTVEKGVPAAEAGRLVVFGIPPDSPETGYGYIESVGKGNVRD----VARFVEKPGLEMAK 184

Query: 183 EFVAAGGYYWNSGMFLFRASRYLEELKKHDADIYD--TCLLALERSQHDGDLVNIDAATF 240
            +VA+G ++WN+G+FLFRA       ++H A I+    C  A   ++  G  + I+   +
Sbjct: 185 AYVASGTFFWNAGIFLFRAGAMRAAFREHQAAIWQKTECAFAAAATEVSGTYLPIE--QY 242

Query: 241 ECCPDNSIDYAVMEKTSRACVVPLSAGWNDVGSWSSIWDVHAKDANGNVTKGDVLVHDSH 300
              P  SIDYA+ME  S   +VP S  W+D+GSW S+ D+   D NGNV  GDV+  D  
Sbjct: 243 STIPSASIDYAIMEHASGIAMVPASFYWSDLGSWQSLLDISPTDGNGNVVIGDVVAIDCE 302

Query: 301 NCLVHGNGKLVSVIGLEDIVVVETKDAMMIAHKDRVQDVKHVVKDLDAQGRSETQ---NH 357
              +   G+L+SVIGL D+ +V T DA  +A   + Q+VK +V+ L+  GR ET+    H
Sbjct: 303 RSYLRSQGRLLSVIGLRDVAIVSTADATFVAPVAKSQEVKRIVEQLEKSGRLETKFTPAH 362

Query: 358 CEVYRP 363
             V +P
Sbjct: 363 ARVLQP 368


Lambda     K      H
   0.319    0.134    0.400 

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: 886
Number of extensions: 42
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: 481
Length of database: 767
Length adjustment: 37
Effective length of query: 444
Effective length of database: 730
Effective search space:   324120
Effective search space used:   324120
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: 53 (25.0 bits)

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

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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:

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:

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:

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:

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