GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Desulfovibrio vulgaris Hildenborough

Align ABC transporter for D-Glucose-6-Phosphate, ATPase component (characterized)
to candidate 208681 DVU3161 ABC transporter, ATP-binding protein

Query= reanno::WCS417:GFF4321
         (386 letters)



>MicrobesOnline__882:208681
          Length = 349

 Score =  274 bits (701), Expect = 2e-78
 Identities = 156/367 (42%), Positives = 221/367 (60%), Gaps = 19/367 (5%)

Query: 1   MATLELRNVNKTYGAGLPDTLKNIELSIKEGEFLILVGPSGCGKSTLMNCIAGLETITGG 60
           M+T+ L  V++ +G      + ++   +++G+ L+L+GPSGCGKST +  IAGLE++T G
Sbjct: 1   MSTIVLDKVSRHWGD--VRAVDDVSFEVEQGDMLVLLGPSGCGKSTTLRLIAGLESVTSG 58

Query: 61  AIMIGDQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKMPQADIDAEVARVA 120
            I+IG +DV+ + P  R +AMVFQSYAL+P ++VR+NI FGL +RK+P A+    + R  
Sbjct: 59  RILIGGRDVTNLPPAQRQLAMVFQSYALFPHLTVRDNILFGLVVRKVPAAERQKRLDRAV 118

Query: 121 KLLQIEHLLNRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180
           ++L +  LL RKPG+LSGGQQQRVA+GRAL     + L DEPLSNLDAKLR EMR E++ 
Sbjct: 119 EILGLGKLLERKPGELSGGQQQRVALGRALVAEAAVCLMDEPLSNLDAKLRQEMRREIRA 178

Query: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKEIYNNPANQFVASFIGSPP 240
           + Q L  T VYVTHDQ EAM++ D++ +M+ G I Q  TP E+Y+ PA  F  SFIG+PP
Sbjct: 179 LQQTLGMTMVYVTHDQTEAMSMADRIILMQGGRIVQNATPTEMYSRPATAFAGSFIGTPP 238

Query: 241 MNFVPLRLQRKDGRLVALLDSGQARCELALNTTEAGLEDRDVILGLRPEQIMLAAGEGDS 300
           MN V L+    DG  VA   SG+  C              D +LG+RPE I +       
Sbjct: 239 MNLVRLQ-GNDDGIRVAGSRSGRVTCHAG----------ADCMLGIRPEHIRIV------ 281

Query: 301 ASSIRAEVQVTEPTGPDTLVFVQLNDTKVCCRLAPDVAPQVGETLTLQFDPSKVLLFDAN 360
               RA V+  E  G ++++  ++   ++   +       VG  + L      V +FDA 
Sbjct: 282 DDGWRAVVESVEYLGSNSVLSCRVGSEELSVVVHGVTDTVVGAEIYLHCPEEHVHIFDAA 341

Query: 361 TGERLGT 367
           TG R  T
Sbjct: 342 TGARHAT 348


Lambda     K      H
   0.318    0.135    0.382 

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: 309
Number of extensions: 11
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: 386
Length of database: 349
Length adjustment: 30
Effective length of query: 356
Effective length of database: 319
Effective search space:   113564
Effective search space used:   113564
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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