GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glk in Cereibacter sphaeroides ATCC 17029

Align Glucokinase; EC 2.7.1.2 (characterized, see rationale)
to candidate WP_011841074.1 RSPH17029_RS07695 glucokinase

Query= uniprot:A8LLL9
         (323 letters)



>NCBI__GCF_000015985.1:WP_011841074.1
          Length = 317

 Score =  341 bits (874), Expect = 2e-98
 Identities = 186/315 (59%), Positives = 219/315 (69%), Gaps = 2/315 (0%)

Query: 4   LRDAP-ALVADIGGTNTRVALADGPVLRAGSVEKYRNADYSSLDSVLRSYLEKMEVAGCS 62
           + DAP  LVADIGGTNTRVALA+G  LR  +  ++RNADY +L  VLR +L         
Sbjct: 1   MADAPLCLVADIGGTNTRVALAEGSRLRPETTRRFRNADYPALAPVLRDFLSVAGSPEID 60

Query: 63  GACVALAGPVRNGIGHLTNLDWRMDEDLLSEATGAPVVALLNDLQAQGFALGHLEAACLR 122
           G CVA AGPVR+G+  LTNL W +D   L  ATGAP VA+LNDLQAQG ALGHL+ A L 
Sbjct: 61  GTCVAAAGPVRDGVALLTNLAWTVDGAELQRATGAPRVAVLNDLQAQGHALGHLDPANLH 120

Query: 123 PVISRPPPAAQETRLMIGLGTGFNAASVLYTPAGRIVTPSEAGHANLPVRTEQELRLCRF 182
            +I  P P      L++G+GTGFNAA V      R+V  SE GHA +PVRT ++LRL  F
Sbjct: 121 VLIPGPTPRRAGPMLVVGVGTGFNAAPVHDVAGLRLVAASECGHAGMPVRTARDLRLAEF 180

Query: 183 VETAHGFPAVEDVLSGRGLERVYNFLSPTPDQPQRLSAAEVMAAAAREERQALDALELFI 242
           V+TAHGF  VEDVLSGRGLER+Y F +       R SAAE+MAA A E   A  A ELF 
Sbjct: 181 VQTAHGFAGVEDVLSGRGLERLYAFTAAEAGLEDRKSAAEIMAAIA-EPGPARAAAELFA 239

Query: 243 GLLGTVAGNLSLIHLPFGGVYLCGGVARHIGPYLGSMGFAEAFANKGRFADFMRDFPVWL 302
            LLG  AGNL+LIHLPFGG+YLCGGVAR    +LG MGFAE F +KGRF+ FM DFPV +
Sbjct: 240 RLLGAEAGNLALIHLPFGGLYLCGGVARAFAAHLGPMGFAENFRDKGRFSAFMDDFPVCI 299

Query: 303 VEDDFAALTGCASFL 317
           VEDD+AALTGCA++L
Sbjct: 300 VEDDYAALTGCAAYL 314


Lambda     K      H
   0.321    0.137    0.412 

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: 395
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: 323
Length of database: 317
Length adjustment: 28
Effective length of query: 295
Effective length of database: 289
Effective search space:    85255
Effective search space used:    85255
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: 48 (23.1 bits)

This GapMind analysis is from Apr 10 2024. 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