GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Klebsiella michiganensis M5al

Align TM0028, component of β-glucoside porter (Conners et al., 2005). Binds cellobiose, laminaribiose (Nanavati et al. 2006). Regulated by cellobiose-responsive repressor BglR (characterized)
to candidate BWI76_RS17225 BWI76_RS17225 oligopeptide ABC transporter ATP-binding protein OppD

Query= TCDB::Q9WXN5
         (330 letters)



>FitnessBrowser__Koxy:BWI76_RS17225
          Length = 337

 Score =  197 bits (501), Expect = 3e-55
 Identities = 115/323 (35%), Positives = 184/323 (56%), Gaps = 13/323 (4%)

Query: 4   ILLKAENVRAYYKLEKVSVKAVDGLSFEILEDEVIGVVGESGCGKTTLSNVIFMNMVKPL 63
           +LL  +++R  +      V AV+ L+F +   E +G+VGESG GK+  +  +       L
Sbjct: 18  LLLDVKDLRVTFGTPDGDVTAVNDLNFNLRAGETLGIVGESGSGKSQTAFALM-----GL 72

Query: 64  TLVDGKIFLRVNGEFVELSSMTRDEVKRKFWGKEITIIPQAAMNALMPTIRMEKYVRHLA 123
              +G+I         ++ ++   E+  K   ++I++I Q  M +L P +R+ + +  + 
Sbjct: 73  LAANGRIGGSATFNGKQILNLPERELN-KLRAEQISMIFQDPMTSLNPYMRVGEQLMEVL 131

Query: 124 ESH-GIDEEELLDKARRRFEEVGLDPLW--IKRYPFELSGGMRQRAVIAIATILNPSLLI 180
             H  + + E  +++ +  + V +      +K YP E SGGMRQR +IA+A +  P LLI
Sbjct: 132 MLHKALSKAEAFEESVKMLDAVKMPEARKRMKMYPHEFSGGMRQRVMIAMALLCRPKLLI 191

Query: 181 ADEPTSALDVVNQKVLLKVLMQMKRQGIVKSIIFITHDIATVRQIADRMIIMYAGKIVEF 240
           ADEPT+ALDV  Q  ++ +L ++KR+    +II ITHD+  V  I D++++MYAG+ +E+
Sbjct: 192 ADEPTTALDVTVQAQIMTLLNELKRE-FNTAIIMITHDLGVVAGICDKVLVMYAGRTMEY 250

Query: 241 APVESLLEKPLHPYTQGLFNSVLTPEPEVKKRGITTIPGAPPNLINPPSGCRFHPRCPHA 300
                +  +P HPY+ GL N+V  P  + +   + TIPG PPNL+  P GC F PRCPHA
Sbjct: 251 GQARDVFYQPSHPYSIGLLNAV--PRLDAEGDALLTIPGNPPNLLRLPKGCPFQPRCPHA 308

Query: 301 MDVCKEKEPPLTEIEPGRRVACW 323
           M++C    PPL E  PGR  AC+
Sbjct: 309 MEIC-NSAPPLEEFAPGRLRACF 330


Lambda     K      H
   0.321    0.138    0.405 

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: 275
Number of extensions: 14
Number of successful extensions: 5
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: 330
Length of database: 337
Length adjustment: 28
Effective length of query: 302
Effective length of database: 309
Effective search space:    93318
Effective search space used:    93318
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 (21.8 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