GapMind for catabolism of small carbon sources

 

Aligments for a candidate for potA in Herbaspirillum seropedicae SmR1

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate HSERO_RS11145 HSERO_RS11145 sulfate ABC transporter ATP-binding protein

Query= TCDB::P31134
         (377 letters)



>lcl|FitnessBrowser__HerbieS:HSERO_RS11145 HSERO_RS11145 sulfate ABC
           transporter ATP-binding protein
          Length = 359

 Score =  235 bits (599), Expect = 2e-66
 Identities = 144/354 (40%), Positives = 206/354 (58%), Gaps = 19/354 (5%)

Query: 10  AKTRKALTPLLEIRNLTKSYDGQHAVDDVSLTIYKGEIFALLGASGCGKSTLLRMLAGFE 69
           A T +     L +R + K +    A+D VSL + +GE+  LLG SGCGK+TLLR +AG E
Sbjct: 3   AATEEDAAVFLSVREVEKRFGSFTALDRVSLEVRRGEMVCLLGPSGCGKTTLLRTIAGLE 62

Query: 70  QPSAGQIMLDGVDLSQVPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAEIASR 129
           +  +G++  DG D+SQ+PP  R   ++FQSYALFP+++V  N+A+GL   ++ + +   R
Sbjct: 63  RQDSGRLHADGRDISQLPPQARDYGILFQSYALFPNLSVADNVAYGL--GRMSRQQKRER 120

Query: 130 VNEMLGLVHMQEFAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRDRMQ 189
           V EML +V +     + P QLSGGQ+QRVALAR+LA  P LLLLDEP+ ALD ++R+ +Q
Sbjct: 121 VTEMLSMVGLDGSQDKYPGQLSGGQQQRVALARALAPSPSLLLLDEPLSALDAQVREHLQ 180

Query: 190 LEVVDILERVGVTCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRYSAEF 249
           LE+  + ++  +T +MVTHDQEEAM MA RIA+M  G+  Q G PE+IY  P T + A+F
Sbjct: 181 LEIRRLQKQFRITTLMVTHDQEEAMVMADRIAVMQHGRIEQFGTPEQIYRRPATPFVADF 240

Query: 250 IGSVNVFEGVLKERQEDGLVLDSPGLVHPLKVDADASVVDNVPVHVALRPEKIMLCEEPP 309
           IG  N     L   +  G  +   GL   L++  D S  D     +  RPE + L  +  
Sbjct: 241 IGQAN----WLPFTRLSGSQVAVGGL--HLEIQPDES--DRASGRLFCRPEAVQLFSDES 292

Query: 310 ANGCNFAVGEVIHIAYLGDLSVYHVRLKS----GQMISAQLQN-AHRHRKGLPT 358
               N  +  V+   YLGD   Y + L +    GQ + A + + AH     L T
Sbjct: 293 C--ANRFLARVVDRIYLGDR--YRLALAADALPGQTLLADVSSQAHERVASLDT 342


Lambda     K      H
   0.321    0.137    0.400 

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: 327
Number of extensions: 10
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: 377
Length of database: 359
Length adjustment: 30
Effective length of query: 347
Effective length of database: 329
Effective search space:   114163
Effective search space used:   114163
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 (21.8 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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