GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagK in Rhodanobacter denitrificans 2APBS1

Align Glucose kinase (characterized, see rationale)
to candidate WP_007510347.1 R2APBS1_RS00795 glucokinase

Query= uniprot:Q8P6S9
         (338 letters)



>NCBI__GCF_000230695.2:WP_007510347.1
          Length = 366

 Score =  313 bits (802), Expect = 4e-90
 Identities = 167/342 (48%), Positives = 222/342 (64%), Gaps = 12/342 (3%)

Query: 4   SSPMEAVAFPRP---ETFVAADVGGTHVRLALACESNDPRKPVTVLDYRKYRCADYPGLA 60
           +S    V  P P   + F+AADVGGTH R+ L   + +   PV+VL Y +Y CA++PGL 
Sbjct: 20  ASAANGVGAPGPGPQQPFLAADVGGTHARIGLVVGNTNGPCPVSVLHYHRYSCAEWPGLT 79

Query: 61  EIMAAFFAELSCAP-------VRRGVIASAGYALEDGRVITANLPWVLAPEQIRQQLGMQ 113
            ++  F A+L+  P       +  G +A AGY L+D  ++  NLPW ++  +IR  LG++
Sbjct: 80  AMLRDFVAQLANTPHAALRSQLHHGAVACAGYVLDDA-IVNGNLPWPVSIREIRDGLGIR 138

Query: 114 ALHLVNDFEAVAYAANYMTGNQVMQLSGPAQ-GAPGPALVLGPGTGLGAALWIPNGGNSV 172
            L ++NDFEA+AYA  ++  ++   +   AQ  A GP LV+GPGTGLG+A+ +P    + 
Sbjct: 139 RLAVINDFEALAYATQFIATDETRPIIETAQPAASGPVLVMGPGTGLGSAVLLPGHPRAQ 198

Query: 173 VLPTEAGHAALAAASDLEVALLQELRRTRTHVATEHFLSGPGLLTLYTALATLRDAPAVH 232
           VL TEAG  +LA  ++ E+ +L+  RR R HV+ E  LSGPGLL LY AL  LR +P   
Sbjct: 199 VLATEAGQVSLAPGNEREIEILRLFRRERAHVSFEDALSGPGLLKLYGALCELRGSPLRL 258

Query: 233 ATPAAVTAAALAGDDVLAHEALQTFCGFMGSVVGDMMLLYGVRSGVYLAGGFLPQIADFI 292
            TPA VT AALAG D  A EAL+ FCG +GS VGD++LLYG R GVYLAGG LPQI  F+
Sbjct: 259 LTPAEVTMAALAGSDGAAVEALEVFCGLLGSFVGDLVLLYGARGGVYLAGGILPQIQPFL 318

Query: 293 ARSDFAARLLDKGPLRPALEQVPVRIVEHGQLGVIGAASWFL 334
             S FA R  +KG +R  L+QVPVR++EHGQLGVIGAA WFL
Sbjct: 319 LASRFAERYFNKGVMRAYLQQVPVRLIEHGQLGVIGAAGWFL 360


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: 314
Number of extensions: 15
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: 366
Length adjustment: 29
Effective length of query: 309
Effective length of database: 337
Effective search space:   104133
Effective search space used:   104133
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 24 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