GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rbsB in Phyllobacterium brassicacearum STM 196

Align D-ribose-binding periplasmic protein; EC 3.6.3.17 (characterized)
to candidate WP_106714416.1 CU102_RS28790 sugar ABC transporter substrate-binding protein

Query= CharProtDB::CH_003593
         (296 letters)



>NCBI__GCF_003010955.1:WP_106714416.1
          Length = 309

 Score =  139 bits (351), Expect = 6e-38
 Identities = 96/304 (31%), Positives = 164/304 (53%), Gaps = 14/304 (4%)

Query: 3   MKKLATLVSAVALSATVSANAMAKDTIALVVSTLNNPFFVSLKDGAQKEADKL-GYNLVV 61
           MKKL   +  VA+SA +S++A A + I + ++  ++ F   L++G Q  A  L G  L V
Sbjct: 1   MKKL---LMTVAVSALMSSSAFAAN-IGVSMALFDDNFLTVLRNGMQDYAKTLDGVTLQV 56

Query: 62  LDSQNNPAKELANVQDLTVRGTKILLINPTDSDAVGNAVKMANQANIPVITLDRQATK-- 119
            D+QN+ AK+ + +Q+        +++NP D+DA     K+A +A IP++ ++R+     
Sbjct: 57  EDAQNDVAKQQSQIQNFIASKVDAIIVNPVDTDATAAMSKIAAEAGIPLVYVNREPVNVN 116

Query: 120 --GEVVSHIASDNVLGGKIAGDYIAKKAGEGAKVIELQGIAGTSAARERGEGFQQAVAAH 177
              E  + +AS+ V  G +    + +      K++ + G     AAR+R +     +A  
Sbjct: 117 ELPEKQAFVASNEVESGTLETKEVCRLLKGKGKIVVMMGELSNQAARQRTKDIHDVIATD 176

Query: 178 K---FNVLASQPADFDRIKGLNVMQNLLTAHPDVQAVFAQNDEMALGALRALQTAGKS-- 232
           +     ++  Q A++ R +G ++M N L+A  +  AV + NDEMA+GA++AL+ AG+S  
Sbjct: 177 ECKGLEIVEEQTANWSRTQGADLMTNWLSAGLEFDAVVSNNDEMAIGAIQALKAAGRSMD 236

Query: 233 DVMVVGFDGTPDGEKAVNDGKLAATIAQLPDQIGAKGVETADKVLKGEKVQAKYPVDLKL 292
            V+V G D T D   A++ G L  T+ Q     G   V+ A K+ KGEKV++K  V  +L
Sbjct: 237 SVVVGGVDATQDALAAMSAGDLDVTVFQNAAGQGQGAVDAALKLSKGEKVESKVYVPFEL 296

Query: 293 VVKQ 296
           V  +
Sbjct: 297 VTPE 300


Lambda     K      H
   0.313    0.129    0.344 

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: 192
Number of extensions: 9
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: 296
Length of database: 309
Length adjustment: 27
Effective length of query: 269
Effective length of database: 282
Effective search space:    75858
Effective search space used:    75858
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 48 (23.1 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