GapMind for catabolism of small carbon sources

 

Alignments for a candidate for proV in Marinobacter adhaerens HP15

Align glycine betaine/l-proline transport atp-binding protein prov (characterized)
to candidate GFF3356 HP15_3298 glycine betaine/L-proline ABC transporter, ATPase subunit

Query= CharProtDB::CH_001555
         (400 letters)



>FitnessBrowser__Marino:GFF3356
          Length = 352

 Score =  290 bits (742), Expect = 4e-83
 Identities = 150/334 (44%), Positives = 220/334 (65%), Gaps = 3/334 (0%)

Query: 3   IKLEIKNLYKIFGEHPQRAFKYIEQGLSKEQILEKTGLSLGVKDASLAIEEGEIFVIMGL 62
           IK+ I+NLYKIFG  P  A +Y+ +G+ K  +LE+    LG++D ++ I +GEI VIMGL
Sbjct: 5   IKISIRNLYKIFGPTPDVALEYVRKGMGKADLLEQQRHVLGLRDINVDIHDGEITVIMGL 64

Query: 63  SGSGKSTMVRLLNRLIEPTRGQVLIDGVDIAKISDAELREVRRKKIAMVFQSFALMPHMT 122
           SGSGKST++R LNRLI+PT G++ +DG DI   S+ +LR++RR++++MVFQ FAL+PH T
Sbjct: 65  SGSGKSTLIRHLNRLIDPTAGEIRVDGEDIMSYSEEQLRKLRRERMSMVFQKFALLPHKT 124

Query: 123 VLDNTAFGMELAGINAEERREKALDALRQVGLENYAHSYPDELSGGMRQRVGLARALAIN 182
           VL+N     ++ G    +    A   L +VGLE   + YP +LSGGM+QRVG+ARAL  +
Sbjct: 125 VLENAGMAKDIRGYTTSDFEADARKWLARVGLEGNEYQYPHQLSGGMQQRVGIARALVSD 184

Query: 183 PDILLMDEAFSALDPLIRTEMQDELVKLQAKHQRTIVFISHDLDEAMRIGDRIAIMQNGE 242
             I+LMDEAFSALDPLIR++MQD L++LQ + Q+TIVFI+HDLDEA+++ D + I+++GE
Sbjct: 185 APIMLMDEAFSALDPLIRSDMQDLLLELQEELQKTIVFITHDLDEALKLADHLVILKDGE 244

Query: 243 VVQVGTPDEILNNPANDYVRTFFRGVDISQVFSAKDIARRTPNGLIRKTPGFGPRSALK- 301
           VVQ G P EIL NP + Y+  F   ++ ++V   + +     +G          +  L+ 
Sbjct: 245 VVQQGDPQEILLNPGDPYIVDFISDINRARVLRVRSVMSPPDDGEATFAGDISEKDNLET 304

Query: 302 --LLQDEDREYGYVIERGNKFVGAVSIDSLKTAL 333
             L  D D    + + R ++ VG + +  L  AL
Sbjct: 305 VLLKSDGDMSLNFRVVRDDQHVGTLHMKDLARAL 338


Lambda     K      H
   0.319    0.137    0.378 

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: 394
Number of extensions: 17
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: 400
Length of database: 352
Length adjustment: 30
Effective length of query: 370
Effective length of database: 322
Effective search space:   119140
Effective search space used:   119140
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: 50 (23.9 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