GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Desulfovibrio vulgaris Miyazaki F

Align ABC transporter for D-Glucose-6-Phosphate, ATPase component (characterized)
to candidate 8499890 DvMF_0655 ABC transporter related (RefSeq)

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



>FitnessBrowser__Miya:8499890
          Length = 350

 Score =  279 bits (714), Expect = 8e-80
 Identities = 158/369 (42%), Positives = 226/369 (61%), Gaps = 23/369 (6%)

Query: 1   MATLELRNVNKTYGAGLPDTLKNIELSIKEGEFLILVGPSGCGKSTLMNCIAGLETITGG 60
           M+ ++L NV++ +G      + ++   +++G  L+L+GPSGCGKST +  IAGLE++T G
Sbjct: 1   MSAIQLLNVSRHWGD--VRAVDDVSFEVEQGTMLVLLGPSGCGKSTTLRLIAGLESVTSG 58

Query: 61  AIMIGDQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKMPQADIDAEVARVA 120
            IMIG++DV+ + P  R +AMVFQSYAL+P ++VRENI FGL +RK+P+A+ +  + R  
Sbjct: 59  RIMIGERDVTHLPPAQRQLAMVFQSYALFPHLTVRENILFGLTVRKVPEAEREKRLTRAV 118

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

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

Query: 241 MNFVPLRLQRKDGRLVALLDSGQARCELALNTTEAGLEDRDVILGLRPEQIMLAAGEGDS 300
           MN V L     D R       G      + + T + ++  D +LG+RPE I +       
Sbjct: 239 MNLVRL----DDAR-------GSVCVAGSRSGTVSVVDSADYVLGIRPEHIRIV------ 281

Query: 301 ASSIRAEVQVTEPTGPDTLVFVQL--NDTKVCCRLAPDVAPQVGETLTLQFDPSKVLLFD 358
               RA V+  E  G  +++  ++   +  V     P +A  VG  + L      + +FD
Sbjct: 282 PEGWRAVVESVEYLGSGSVLGCRVGGEELSVVVDGVPTIA--VGAEIYLHCPDEHIHIFD 339

Query: 359 ANTGERLGT 367
           A TGER GT
Sbjct: 340 AKTGERRGT 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: 317
Number of extensions: 11
Number of successful extensions: 3
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: 350
Length adjustment: 30
Effective length of query: 356
Effective length of database: 320
Effective search space:   113920
Effective search space used:   113920
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