GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK1 in Desulfovibrio vulgaris Hildenborough

Align MalK; aka Sugar ABC transporter, ATP-binding protein, component of The maltose, maltotriose, mannotetraose (MalE1)/maltose, maltotriose, trehalose (MalE2) porter (Nanavati et al., 2005). For MalG1 (823aas) and MalG2 (833aas), the C-terminal transmembrane domain with 6 putative TMSs is preceded by a single N-terminal TMS and a large (600 residue) hydrophilic region showing sequence similarity to MLP1 and 2 (9.A.14; e-12 & e-7) as well as other proteins (characterized)
to candidate 209027 DVU0098 polyamine ABC transporter, ATP-binding protein

Query= TCDB::Q9X103
         (369 letters)



>MicrobesOnline__882:209027
          Length = 368

 Score =  259 bits (661), Expect = 1e-73
 Identities = 139/291 (47%), Positives = 197/291 (67%), Gaps = 13/291 (4%)

Query: 6   VVLENVTKVYENKVVAVKNANLVVEDKEFVVLLGPSGCGKTTTLRMIAGLEEITDGKIYI 65
           + L  VTK +E+   A+ N +L + + EF+ LLGPSGCGKTT LR+I+G E+   G I +
Sbjct: 8   IELRGVTKNFED-TCALDNIDLEIRNGEFLTLLGPSGCGKTTILRLISGFEKPDAGVITL 66

Query: 66  DGKVVNDVEPKDRDIAMVFQNYALYPHMTVYENMAFGLKLRKYPKDEIDRRVREAAKILG 125
            G+ ++D  P+ R +  VFQNYAL+PHM+V EN+ FGL++++ PKDEI RRV +A +++ 
Sbjct: 67  KGQRMDDAPPEARQVNTVFQNYALFPHMSVRENVGFGLRMQRRPKDEIARRVHDALRMVH 126

Query: 126 IENLLDRKPRQLSGGQRQRVAVGRAIVRNPKVFLFDEPLSNLDAKLRVQMRSELKKLHHR 185
           +E   DR+PRQLSGGQ+QRVA+ RA+V NP V L DEP S LD KLR QM+ E+K L  +
Sbjct: 127 LEAHADRRPRQLSGGQQQRVAIARAVVNNPLVLLLDEPFSALDYKLRKQMQLEIKHLQRQ 186

Query: 186 LQATIIYVTHDQVEAMTMADKIVVMKDGEIQQIGTPHEIYNSPANVFVAGFIGSPPMNFV 245
           L  T ++VTHDQ EA  M+D++VVM DG+I+QIG+P EIY  PAN++VA F+G   +N +
Sbjct: 187 LGITFVFVTHDQEEAFAMSDRVVVMNDGKIEQIGSPQEIYEEPANLYVARFVGE--INIL 244

Query: 246 NARVVRGEG-GLW---IQASGFKVKVPKEFEDKLANYIDKEIIFGIRPEDI 292
           NA +    G GL+   I+   F ++  + F        DK  +  +RPED+
Sbjct: 245 NAVIAANHGDGLYDAVIEGVTFPIRSQRTFAPG-----DKVNVL-LRPEDL 289


Lambda     K      H
   0.319    0.138    0.387 

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: 374
Number of extensions: 14
Number of successful extensions: 1
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: 369
Length of database: 368
Length adjustment: 30
Effective length of query: 339
Effective length of database: 338
Effective search space:   114582
Effective search space used:   114582
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