GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gntC in Cereibacter sphaeroides ATCC 17029

Align TRAP-type periplasmic solute-binding protein (characterized, see rationale)
to candidate WP_011841463.1 RSPH17029_RS10770 TRAP transporter substrate-binding protein

Query= uniprot:Q930R1
         (334 letters)



>NCBI__GCF_000015985.1:WP_011841463.1
          Length = 325

 Score =  189 bits (480), Expect = 8e-53
 Identities = 112/313 (35%), Positives = 173/313 (55%), Gaps = 5/313 (1%)

Query: 1   MRKLLLATTAIAFGLSAAAPAFAEFNDRNIRVSNGINEDHPVGNGIKAMQACLDQKSGGK 60
           M+K ++AT   +  L  AAPAFAE  +  +R S+   + +P   G+K M     + S G+
Sbjct: 1   MKKTMIATLLASAAL--AAPAFAEC-EVTLRSSDTHPDGYPTVEGVKFMAERAKELSNGR 57

Query: 61  LKLTAFWGGALGGDLQATQALRSGVQEAVVTSSSPLVGIIPALGVFDLPFLFANAQEAYT 120
           + +  F    LG +    +  + GV + V  S      I+P   +  LP+LF + +  + 
Sbjct: 58  ICIEVFPSSQLGEEKDTIEQTQFGVIDMVRASFGSFNDIVPEAQLLSLPYLFRSEEHLHN 117

Query: 121 VLDGDFGDMMNEKLEAAGLVNLAYWENGFRNLSNSVRPVTKWEDFEGMKVRVMQNNIFLD 180
           V+DG  GD + +  EA  L+ +AY++ G R+  NS +P+TK ED +GMK RVMQ+++F+D
Sbjct: 118 VMDGPIGDELAKAFEAKDLIAVAYYDGGSRSFYNSQKPITKVEDLKGMKFRVMQSDVFVD 177

Query: 181 TFQNLGANATPMAFGEVFSALETKAIDAQENPYVTIDTSKFFEVQKYVTETNHAYTPFLF 240
               LGANATPM +GEV+S+++T  ID  EN + + D+S  FEV KY T   H   P L 
Sbjct: 178 MMSALGANATPMPYGEVYSSIQTGVIDGAENNWPSYDSSGHFEVAKYYTLDQHLMVPELV 237

Query: 241 LFSKPIFDSYTPEEQAALRECAVVGRDEERKVIQDLNKKSLEKIKEAGLEVNTLSAEEQA 300
             SK  +D+ +PE+Q  LR+ A      +RK+  +  K S EK+  +G EV  +   ++ 
Sbjct: 238 AISKIKWDALSPEDQQVLRQAAEESEPVQRKLWAEQEKASEEKVVASGAEV--VREIDKT 295

Query: 301 RIREKSMVVYEKH 313
              E    VYEK+
Sbjct: 296 PFIEAMAPVYEKY 308


Lambda     K      H
   0.317    0.133    0.374 

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: 239
Number of extensions: 9
Number of successful extensions: 1
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: 334
Length of database: 325
Length adjustment: 28
Effective length of query: 306
Effective length of database: 297
Effective search space:    90882
Effective search space used:    90882
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: 49 (23.5 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