GapMind for catabolism of small carbon sources

 

Alignments for a candidate for garK in Shewanella sp. ANA-3

Align Glycerate 3-kinase; D-Glycerate-3-kinase; Glycerate kinase 2; GK2; EC 2.7.1.31 (characterized)
to candidate 7025534 Shewana3_2685 glycerate kinase (RefSeq)

Query= SwissProt::P77364
         (381 letters)



>FitnessBrowser__ANA3:7025534
          Length = 381

 Score =  408 bits (1048), Expect = e-118
 Identities = 212/380 (55%), Positives = 266/380 (70%), Gaps = 3/380 (0%)

Query: 1   MKIVIAPDSFKESLSAEKCCQAIKAGFSTLFPDANYICLPIADGGEGTVDAMVAATGGNI 60
           MKIVIAPDSFKESLSA     AI+ G + + PD   + +P+ADGGEGTV +MV ATGG+I
Sbjct: 1   MKIVIAPDSFKESLSALDVANAIEQGLTQVIPDCEIVKIPVADGGEGTVQSMVDATGGSI 60

Query: 61  VTLEVCGPMGEKVNAFYGLTGD---GKTAVIEMAAASGLMLVAPEKRNPLLASSFGTGEL 117
           V LEV GP+G KV A YG+ G    G  AVIEMA+ASGL  V  + RNPLL +S+GTGEL
Sbjct: 61  VNLEVMGPLGHKVKAHYGILGQQAKGTIAVIEMASASGLHHVPRDLRNPLLTTSYGTGEL 120

Query: 118 IRHALDNDIRHIILGIGGSATVDGGMGMAQALGVRFLDADGQALAANGGNLARVASIEMD 177
           I  AL+  I+HIILG+GGSAT DGG GMAQAL +  LD  G+ L+A G  L+++ASI++ 
Sbjct: 121 ICDALNRGIKHIILGLGGSATNDGGAGMAQALDILLLDKQGKTLSAGGAALSQLASIDIS 180

Query: 178 ECDPRLANCHIEVACDVDNPLVGARGAAAVFGPQKGATPEMVEELEQGLQNYARVLQQQT 237
              P L  C  EVACDVDNPL G RGA+A+FGPQKGAT EMV  L+  L +YA V+ Q  
Sbjct: 181 HAHPLLKECTFEVACDVDNPLCGERGASAIFGPQKGATSEMVSTLDAALSHYADVIAQSG 240

Query: 238 EINVCQMAGGGAAGGMGIAAAVFLNADIKPGIEIVLNAVNLAQAVQGAALVITGEGRIDS 297
             +    AG GAAGGMG+    FL A++KPG+EIV+  V LA  ++GA LVITGEGRID 
Sbjct: 241 VTDHRNQAGAGAAGGMGLGVMAFLGAELKPGVEIVMQTVGLADKIRGADLVITGEGRIDG 300

Query: 298 QTAGGKAPLGVASVAKQFNVPVIGIAGVLGDGVEVVHQYGIDAVFSILPRLAPLAEVLAS 357
           QT  GK P+GV   A+  N+P IG+AG LGD    V + G+ A+F I+P L+PL +VLA+
Sbjct: 301 QTIFGKTPMGVLKQAQLQNIPTIGVAGCLGDNANAVLEQGMAAIFPIIPHLSPLDDVLAN 360

Query: 358 GETNLFNSARNIACAIKIGQ 377
            +TNL N+ARNI   + +G+
Sbjct: 361 AKTNLTNTARNIGAVLMLGK 380


Lambda     K      H
   0.318    0.136    0.391 

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: 491
Number of extensions: 31
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: 381
Length of database: 381
Length adjustment: 30
Effective length of query: 351
Effective length of database: 351
Effective search space:   123201
Effective search space used:   123201
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: 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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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