Alignments for a candidate for nupA in Azospirillum brasilense Sp245

GapMind for catabolism of small carbon sources

Alignments for a candidate for nupA in Azospirillum brasilense Sp245

Align Purine/cytidine ABC transporter ATP-binding protein, component of General nucleoside uptake porter, NupABC/BmpA (transports all common nucleosides as well as 5-fluorocytidine, inosine, deoxyuridine and xanthosine) (Martinussen et al., 2010) (Most similar to 3.A.1.2.12). NupA is 506aas with two ABC (C) domains. NupB has 8 predicted TMSs, NupC has 9 or 10 predicted TMSs in a 4 + 1 (or 2) + 4 arrangement (characterized)
to candidate AZOBR_RS06950 AZOBR_RS06950 ABC transporter

Query= TCDB::A2RKA7
         (506 letters)



>FitnessBrowser__azobra:AZOBR_RS06950
          Length = 520

 Score =  360 bits (925), Expect = e-104
 Identities = 206/497 (41%), Positives = 305/497 (61%), Gaps = 6/497 (1%)

Query: 7   IQMIDVTKRFGDFVANDKVNLELKKGEIHALLGENGAGKSTLMNILSGLLEPSEGEVHVK 66
           +++  +TKRF   +AND+V+L L+ GEIHALLGENGAGKSTL+ I+ G+L    G +   
Sbjct: 13  LELRGITKRFPGCLANDQVDLVLRPGEIHALLGENGAGKSTLVKIIYGVLHADAGRIQWN 72

Query: 67  GKLENIDSPSKAANLGIGMVHQHFMLVDAFTVTENIILGNEVTKGINLDLKTAKKKILEL 126
           G   +I  P+ A  LGIGMV QHF L D  TV ENI LG +    I+        +I E+
Sbjct: 73  GHDTHIPDPAGARRLGIGMVFQHFSLFDTLTVAENISLGLDQPGPID----ALSARIAEV 128

Query: 127 SERYGLSVEPDALIRDISVGQQQRVEILKTLYRGADILIFDEPTAVLTPAEITELMQIMK 186
           SERYGLS++P   + ++SVG++QRVEI++ L +   +LI DEPT+VLTP E T L + ++
Sbjct: 129 SERYGLSLDPRRHVHNLSVGERQRVEIVRCLLQDPKLLIMDEPTSVLTPQEATRLFETLR 188

Query: 187 NLIKEGKSIILITHKLDEIRAVADRITVIRRGKSIDTVELGDKTNQELAELMVGRSVSFI 246
            L  EG +I+ I+HKL+EIRA+ D  TV+R G+ + + +   +T + LAE+M+G  +S  
Sbjct: 189 RLAAEGCTILYISHKLEEIRALCDTATVLRGGRVVGSCDPRRETARSLAEMMIGTELSTP 248

Query: 247 TEKAAAQPKDVVLEIKDLNI-KESRGSLKVKGLSLDVRAGEIVGVAGIDGNGQTELVKAI 305
                 +     L+++ L+   ++  +  +K +S +VRAGEI+G+AG+ GNGQ EL+ A+
Sbjct: 249 ERLPQGEAGAAKLQVRHLSTTSDNPFATNLKDVSFEVRAGEILGIAGVAGNGQAELMAAL 308

Query: 306 TGLTKV-DSGSIKLHNKDITNQRPRKITEQSVGHVPEDRHRDGLVLEMTVAENIALQTYY 364
           +G   V D  S+ +  +   +  PR+     +  VPE+R   G V E++++EN  L  Y 
Sbjct: 309 SGEALVPDPASVAIEGRPAGHLGPRERRLLGLAFVPEERLGRGAVPELSLSENALLSGYA 368

Query: 365 KPPMSKYGFLDYNKINSHARELMEEFDVRGAGEWVSASSLSGGNQQKAIIAREIDRNPDL 424
           + P+ + G + + +  S+A  ++  F+V   G    A SLSGGN QK II REI + P L
Sbjct: 369 REPLVRSGLVHFGRARSYAERIIGAFNVVTHGHRAEARSLSGGNLQKFIIGREILQKPRL 428

Query: 425 LIVSQPTRGLDVGAIEYIHKRLIQARDEGKAVLVISFELDEILNVSDRIAVIHDGQIQGI 484
           L+V QPT G+D GA   IH+ LI     G AVLVIS +LDE+  +SDRIAV+  G +   
Sbjct: 429 LVVGQPTWGVDAGAAAAIHRALIDLARAGAAVLVISQDLDELFVLSDRIAVLFHGHLSES 488

Query: 485 VSPETTTKQELGILMVG 501
                T+ +E+G+LM G
Sbjct: 489 RPTHHTSVEEIGLLMGG 505



 Score = 78.2 bits (191), Expect = 7e-19
 Identities = 67/247 (27%), Positives = 115/247 (46%), Gaps = 13/247 (5%)

Query: 259 LEIKDLNIKESRGSLKVKGLSLDVRAGEIVGVAGIDGNGQTELVKAITGLTKVDSGSIKL 318
           LE++ +  K   G L    + L +R GEI  + G +G G++ LVK I G+   D+G I+ 
Sbjct: 13  LELRGIT-KRFPGCLANDQVDLVLRPGEIHALLGENGAGKSTLVKIIYGVLHADAGRIQW 71

Query: 319 HNKDITNQRPRKITEQSVGHVPEDRHRDGLVLEMTVAENIALQTYYKPPMSKYGFLDYNK 378
           +  D     P       +G V +      L   +TVAENI+L      P+        + 
Sbjct: 72  NGHDTHIPDPAGARRLGIGMVFQ---HFSLFDTLTVAENISLGLDQPGPI--------DA 120

Query: 379 INSHARELMEEFDVRGAGEWVSASSLSGGNQQKAIIAREIDRNPDLLIVSQPTRGLDVGA 438
           +++   E+ E + +          +LS G +Q+  I R + ++P LLI+ +PT  L    
Sbjct: 121 LSARIAEVSERYGL-SLDPRRHVHNLSVGERQRVEIVRCLLQDPKLLIMDEPTSVLTPQE 179

Query: 439 IEYIHKRLIQARDEGKAVLVISFELDEILNVSDRIAVIHDGQIQGIVSPETTTKQELGIL 498
              + + L +   EG  +L IS +L+EI  + D   V+  G++ G   P   T + L  +
Sbjct: 180 ATRLFETLRRLAAEGCTILYISHKLEEIRALCDTATVLRGGRVVGSCDPRRETARSLAEM 239

Query: 499 MVGGNIN 505
           M+G  ++
Sbjct: 240 MIGTELS 246


Lambda     K      H
   0.315    0.135    0.365 

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: 613
Number of extensions: 27
Number of successful extensions: 8
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 506
Length of database: 520
Length adjustment: 35
Effective length of query: 471
Effective length of database: 485
Effective search space:   228435
Effective search space used:   228435
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: 42 (22.0 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources