GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagK in Pseudomonas stutzeri RCH2

Align Glucose kinase (characterized, see rationale)
to candidate GFF836 Psest_0850 glucokinase, proteobacterial type

Query= uniprot:Q8P6S9
         (338 letters)



>FitnessBrowser__psRCH2:GFF836
          Length = 319

 Score =  155 bits (393), Expect = 1e-42
 Identities = 121/315 (38%), Positives = 153/315 (48%), Gaps = 14/315 (4%)

Query: 19  VAADVGGTHVRLALACESNDPRKPVTVLDYRKYRCADYPGLAEIMAAFFAELSCAP--VR 76
           +  D+GGT+ R AL  +S        +   R    AD+      +  + A L  AP  V 
Sbjct: 5   LVGDIGGTNARFALWRDSR-------LESVRVLAAADFATPEMAVEYYLASLGLAPGSVE 57

Query: 77  RGVIASAGYALEDGRVITANLPWVLAPEQIRQQLGMQALHLVNDFEAVAYAANYM-TGNQ 135
              +A AG    +    T N  W L        L M  L L+NDF A+A     +    +
Sbjct: 58  AACLACAGPVKGEQFTFTNN-HWRLTRSDFCGALQMGELLLINDFAAMALGMTRVGEAGR 116

Query: 136 VMQLSGPAQGAPGPALVLGPGTGLGAALWIPNGGNSV-VLPTEAGHAALAAASDLEVALL 194
            M  +G A+    PALV+GPGTGLG A  +P GG S   LP E GH  L  A   E AL 
Sbjct: 117 RMICAGEAE-PDAPALVIGPGTGLGVAGLLPLGGGSWRALPGEGGHVDLPVADAHEAALW 175

Query: 195 QELRRTRTHVATEHFLSGPGLLTLYTALATLRDAPAVHATPAAVTAAALAGDDVLAHEAL 254
           Q L     HV  E  LSG GLL LY  + T+       A+PA VTAAALAGD V A   L
Sbjct: 176 QMLFAQLGHVRAEDVLSGGGLLLLYRTVCTVAGLAPRLASPAEVTAAALAGDHV-AVATL 234

Query: 255 QTFCGFMGSVVGDMMLLYGVRSGVYLAGGFLPQIADFIARSDFAARLLDKGPLRPALEQV 314
           + FC ++G V G+ +L  G R GVY+ GG +P+ ADF A S FA     KG +   L  V
Sbjct: 235 EQFCVWLGRVAGNNVLTLGARGGVYIVGGVVPRFADFFAASGFARGFTSKGCMSRYLGDV 294

Query: 315 PVRIVEHGQLGVIGA 329
           PV +V     G+ GA
Sbjct: 295 PVWLVTAEFPGLEGA 309


Lambda     K      H
   0.321    0.136    0.407 

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: 252
Number of extensions: 12
Number of successful extensions: 4
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: 338
Length of database: 319
Length adjustment: 28
Effective length of query: 310
Effective length of database: 291
Effective search space:    90210
Effective search space used:    90210
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 (21.9 bits)
S2: 49 (23.5 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