GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfQ in Sinorhizobium meliloti 1021

Align Galactofuranose-binding protein YtfQ (characterized)
to candidate SM_b21345 SM_b21345 sugar uptake ABC transporter substrate-binding protein precursor

Query= SwissProt::P39325
         (318 letters)



>FitnessBrowser__Smeli:SM_b21345
          Length = 327

 Score =  221 bits (562), Expect = 2e-62
 Identities = 131/301 (43%), Positives = 174/301 (57%), Gaps = 8/301 (2%)

Query: 13  AAMSSMALAAPLTVGFSQVGSESGWRAAETNVAKSEAEKRGITLKIADGQQKQENQIKAV 72
           A +  +A      VGF+Q  S + WR A+TN  K+EAEK G  L   D       Q+  V
Sbjct: 28  AELPKLAQKETYKVGFAQTESNNPWRIAQTNSMKAEAEKLGHQLVYTDAAGSAAKQVADV 87

Query: 73  RSFVAQGVDAIFIAPVVATGWEPVLKEAKDAEIPVFLLDRSID---VKDKSLYMTTVTAD 129
            S +AQGVD IF+AP       P +  AK A IPV LLDRS+D    K    Y+T + +D
Sbjct: 88  NSMIAQGVDLIFLAPREEKPLIPAVMAAKKAGIPVILLDRSVDPSLAKAGEDYVTFIGSD 147

Query: 130 NILEGKLIGDWLVKEVNGKPCNVVELQGTVGASVAIDRKKGFAEAIKNAPNIKIIRSQSG 189
            I EGK I +WLVK  NGK   ++EL+GT G+S A DRKKGF E IK A   +I+ SQSG
Sbjct: 148 FIEEGKRIAEWLVKNANGK-SKIIELEGTTGSSPANDRKKGFDETIKAAGGFEIVASQSG 206

Query: 190 DFTRSKGKEVMESFIKAENNGKNICMVYAHNDDMVIGAIQAIKEAGLKPGKDILTGSIDG 249
           DF R KG++V E+ ++A  +     +VYAHND+M IGAI AI+ AG  PGKD+L  SIDG
Sbjct: 207 DFARDKGRQVAEALLQAHPDAD---IVYAHNDEMAIGAIAAIEAAGKVPGKDVLVLSIDG 263

Query: 250 VPDIYKAMMDGEANASVELTPNMAGPAFDALEKYKKDGTMPEKLTLTKSTLYLPDTAKEE 309
             +  +A++DG+  A VE  P     AF+ + +Y K G   + + + +   Y    A  E
Sbjct: 264 GKEAVQAVIDGKIAAVVECNPRFGPKAFETMLRYAK-GEKIDPMVINEDKFYDSSNAAAE 322

Query: 310 L 310
           L
Sbjct: 323 L 323


Lambda     K      H
   0.313    0.130    0.363 

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: 267
Number of extensions: 15
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: 318
Length of database: 327
Length adjustment: 28
Effective length of query: 290
Effective length of database: 299
Effective search space:    86710
Effective search space used:    86710
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 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