GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Shewanella loihica PV-4

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 5210054 Shew_2501 oligopeptide/dipeptide ABC transporter, ATPase subunit (RefSeq)

Query= TCDB::Q9WXN5
         (330 letters)



>FitnessBrowser__PV4:5210054
          Length = 337

 Score =  137 bits (344), Expect = 5e-37
 Identities = 95/294 (32%), Positives = 161/294 (54%), Gaps = 20/294 (6%)

Query: 22  VKAVDGLSFEILEDEVIGVVGESGCGKTTLSNVIFMNMVKPLTLVDGKIFLRVNGEFVEL 81
           VKA++ +S  +   EV G+VGESG G+T L+  I        T+   ++    +G+   L
Sbjct: 20  VKALERVSLTLNPGEVHGLVGESGSGRTLLAKAILGIPGHNWTIQADRMMW--DGQ--NL 75

Query: 82  SSMTRDEVKRKFWGKEITIIPQAAMNALMPTIRM-EKYVRHLAES-------HGIDEEEL 133
             M+  E +R   G E+ +I Q  +++L P I +  + +  + E+        G D+ + 
Sbjct: 76  MDMSPSE-RRVLMGSEMAMIFQDPISSLDPAIAVGTQIIEAMPENKELPWWKRGSDKRK- 133

Query: 134 LDKARRRFEEVGLDPLW--IKRYPFELSGGMRQRAVIAIATILNPSLLIADEPTSALDVV 191
             KA++   +VG+      +  Y +ELS G  Q+ +IAIA    P LLIADEPT++++V 
Sbjct: 134 --KAQQWLHKVGIKETQKIMSSYAWELSDGECQKVMIAIAVANQPRLLIADEPTNSMEVR 191

Query: 192 NQKVLLKVLMQMKRQGIVKSIIFITHDIATVRQIADRMIIMYAGKIVEFAPVESLLEKPL 251
            Q  + ++L ++ +   V SI+ I+H++ T+ Q  DR+ +MY+G+++E      ++  P 
Sbjct: 192 TQAQIFRLLSKLNQLQNV-SILLISHELETLSQWCDRLTVMYSGQVMESGVTSDVIANPY 250

Query: 252 HPYTQGLFNSVLT-PEPEVKKRGITTIPGAPPNLINPPSGCRFHPRCPHAMDVC 304
           HPYT+ L +++     PE  K  + T+PG+ P L + P GCR  PRCP A  +C
Sbjct: 251 HPYTKALLDNIPDYSNPEHHKTMMQTLPGSAPALQHLPIGCRLGPRCPQAQKLC 304


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: 253
Number of extensions: 12
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: 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.

Links

Downloads

Related tools

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