GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Desulfovibrio vulgaris Miyazaki F

Align spermidine/putrescine ABC transporter, ATP-binding protein PotA; EC 3.6.3.31 (characterized)
to candidate 8500849 DvMF_1587 ABC transporter related (RefSeq)

Query= CharProtDB::CH_024626
         (378 letters)



>FitnessBrowser__Miya:8500849
          Length = 366

 Score =  237 bits (605), Expect = 3e-67
 Identities = 143/326 (43%), Positives = 195/326 (59%), Gaps = 22/326 (6%)

Query: 18  VQLAGIRKCFDGKEVIPQLDLTINNGEFLTLLGPSGCGKTTVLRLIAGLETVDSGRIMLD 77
           + LAGI K +    V+  L LT+N+GE  TLLGPSGCGKT +LRLIAG ET D+G I + 
Sbjct: 4   ITLAGIGKAYGAHAVLDGLSLTVNHGECFTLLGPSGCGKTVLLRLIAGFETPDAGTISIG 63

Query: 78  NEDITH------VPAENRYVNTVFQSYALFPHMTVFENVAFGLRMQKTPAAEITPRVMEA 131
            E ++       VP + R +  VFQ YA++PHM+V +N+ + L++   PAAE T +V+E 
Sbjct: 64  GEPVSDAVTGDCVPPDARDLGVVFQDYAVWPHMSVADNIGYPLKLAGLPAAERTRQVLET 123

Query: 132 LRMVQLETFAQRKPHQLSGGQQQRVAIARAVVNKPRLLLLDESLSALDYKLRKQMQNELK 191
           + MV L     R P QLSGGQQQRVA+ARA+V +P L+LLDE L  LD  LR++M+ E+K
Sbjct: 124 VEMVNLTGLENRMPSQLSGGQQQRVALARALVGRPSLMLLDEPLCNLDANLREEMRFEIK 183

Query: 192 ALQRKLGITFVFVTHDQEEALTMSDRIVVM-RDGRIEQDGTPREIYEEPKNLFVAGFIGE 250
            LQR LGIT ++VTHDQE AL +SDR+ +M   G I Q GTP EI+E P + FV  F+G 
Sbjct: 184 ELQRTLGITILYVTHDQEIALAISDRLAIMDHAGAIRQVGTPWEIFERPADEFVFRFMGV 243

Query: 251 INMFNATVIERLDEQRVRANVEGRECNIYVNFAVEPGQKLHVL--LRPEDLRVEEINDDN 308
            N   A    R     + A  E       V + +  G   H +   RP D+R+    D  
Sbjct: 244 ANFLPA---RRRGMAMLAAGGEQP-----VPWGLPDGDAEHWMAGFRPSDVRLARQGD-- 293

Query: 309 HAEGLIGYVRERNYKGMTLESVVELE 334
              GL G VR  ++ G   + ++E++
Sbjct: 294 ---GLRGTVRRASFLGAMTDYLIEVD 316


Lambda     K      H
   0.319    0.136    0.385 

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: 305
Number of extensions: 14
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: 378
Length of database: 366
Length adjustment: 30
Effective length of query: 348
Effective length of database: 336
Effective search space:   116928
Effective search space used:   116928
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 (21.7 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