GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Azospirillum brasilense Sp245

Align Spermidine/putrescine import ATP-binding protein PotA, component of The spermidine/putrescine uptake porter, PotABCD (characterized)
to candidate AZOBR_RS26295 AZOBR_RS26295 branched-chain amino acid ABC transporter substrate-binding protein

Query= TCDB::Q97Q42
         (385 letters)



>FitnessBrowser__azobra:AZOBR_RS26295
          Length = 354

 Score =  254 bits (650), Expect = 2e-72
 Identities = 153/352 (43%), Positives = 216/352 (61%), Gaps = 24/352 (6%)

Query: 6   IEFKNVSKVFEDSNTKVLKDINFELEEGKFYTLLGASGSGKSTILNIIAGLLDATTGDIM 65
           IEF++V K +   + K L D +  +  G+F T+LG+SGSGK+T LN +AG   A +GDI 
Sbjct: 1   IEFQSVRKAY--GSVKALHDFSLTIRPGEFLTILGSSGSGKTTALNALAGFSTADSGDIR 58

Query: 66  LDGVRINDIPTNKRDVHTVFQSYALFPHMNVFENVAFPLRLRKIDKKEIEQRVAEVLKMV 125
           +DG  + D P  +R++  VFQ+Y+LFPHM+VF+N+AFPLR+R++ +++I++RV  VL++V
Sbjct: 59  IDGRSVIDEPPERRNLGMVFQNYSLFPHMSVFDNIAFPLRMRRMPRRDIKERVERVLEIV 118

Query: 126 QLEGYEKRSIRKLSGGQRQRVAIARAIINQPRVVLLDEPLSALDLKLRTDMQYELRELQQ 185
           +L     R  R LSGGQ+QRVA ARAI+ +P V+L+DEPL ALDLKLR  +Q+E++E+Q 
Sbjct: 119 RLGPLAGRMPRDLSGGQQQRVAFARAIVFEPPVLLMDEPLGALDLKLREALQFEIKEIQH 178

Query: 186 RLGITFVFVTHDQEEALAMSDWIFVMNDGEIVQSGTPVDIYDEPINHFVATFIGESNIL- 244
           +LG T V+VTHDQ EALAMS  I V+ DG I Q GTP ++YD P + FVA FIG++N+L 
Sbjct: 179 QLGCTVVYVTHDQREALAMSSRIVVLRDGRIEQVGTPSEMYDAPQSRFVADFIGQTNLLA 238

Query: 245 -----PGTM-IEDYLVEFNGKRFEAVDGGMKPNEPVEVVIRPEDLRITLPEEG---KLQV 295
                PG++ I +  V +    F A  G    +      IRPE L+   P EG    + V
Sbjct: 239 ADVAQPGSVAIPELGVTYRENAFTARPGSWYAS------IRPEKLQ-RRPAEGPDIAVSV 291

Query: 296 KVDTQLFRGVHYEIIAYDELG-----NEWMIHSTRKAIVGEEIGLDFEPEDI 342
            +   +F G   E  A  + G      E      R    GE   L   P D+
Sbjct: 292 TIQEAVFLGDVIEYSARTDHGALIHFREQRRDRDRIPERGETANLVLRPSDV 343


Lambda     K      H
   0.318    0.138    0.386 

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: 321
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: 385
Length of database: 354
Length adjustment: 30
Effective length of query: 355
Effective length of database: 324
Effective search space:   115020
Effective search space used:   115020
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