GapMind for catabolism of small carbon sources

 

Aligments for a candidate for TM1749 in Desulfovibrio vulgaris Miyazaki F

Align TM1749, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate 8501089 DvMF_1825 oligopeptide/dipeptide ABC transporter, ATPase subunit (RefSeq)

Query= TCDB::Q9X271
         (324 letters)



>lcl|FitnessBrowser__Miya:8501089 DvMF_1825 oligopeptide/dipeptide
           ABC transporter, ATPase subunit (RefSeq)
          Length = 339

 Score =  208 bits (529), Expect = 2e-58
 Identities = 109/303 (35%), Positives = 179/303 (59%), Gaps = 8/303 (2%)

Query: 16  RVEGIVKAVDGISYKLNKGESLGIVGESGSGKSVSVLSLLRLINRNGRIVDGEAIFLGKD 75
           R   +V AV+ +S+ +  GE+L +VGESG GKS    +++ L    G    GE ++ G+ 
Sbjct: 37  RKRTVVHAVNDVSFDILPGETLSVVGESGCGKSTLARTVIGLYRATG----GEILYRGER 92

Query: 76  LLKLNKEELRNIRGKDISIIFQNPMTSLNPIIRVGIQVMEPIIWHRL-MKNEEARERAIE 134
           +  L+   +   R + + ++FQ+P  SLNP ++V   + EP+ +H   + + + R R  +
Sbjct: 93  IDNLSDNGMLPYRTR-MQMVFQDPYASLNPRMKVREILEEPVRFHNPGISDADVRARVAD 151

Query: 135 LLERVGIPESPKRFLNYPFQFSGGMRQRVMIAMALACHPKLLIADEPTTALDVTIQAQIM 194
           ++E+VG+  +P   + YP +FSGG RQR+ IA AL   P+ ++ADEP +ALDV+IQAQ++
Sbjct: 152 VMEQVGV--NPLWGVRYPHEFSGGQRQRISIARALVVDPEFIVADEPISALDVSIQAQVL 209

Query: 195 ELLQELKEEYGMSVIFITHDLSVATNFCDRIITMYAGKIVEEAPVEEILKTPLHPYTKGL 254
            L+ +++E+  ++ +FI+HDLSV  +   R+  MY G + E A  E++   P HPYT+ L
Sbjct: 210 NLMMDMQEKRNLTYLFISHDLSVVEHISTRVAVMYLGSLCELASAEDLFGNPRHPYTRAL 269

Query: 255 LNSTLEIGSRGKKLVPIPGNPPNPTKHPSGCKFHPRCSFAMEICQREEPPLVNISENHRV 314
           L++   IG +    + + G+ P P   P+GC FH RC  A   C +E P    +    +V
Sbjct: 270 LSAIPRIGGKAAGHIKLSGDVPTPINLPTGCVFHGRCQHANARCMQEVPKARQLEGGAQV 329

Query: 315 ACH 317
           ACH
Sbjct: 330 ACH 332


Lambda     K      H
   0.320    0.139    0.401 

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: 281
Number of extensions: 13
Number of successful extensions: 2
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: 324
Length of database: 339
Length adjustment: 28
Effective length of query: 296
Effective length of database: 311
Effective search space:    92056
Effective search space used:    92056
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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