GapMind for catabolism of small carbon sources

 

Alignments for a candidate for AZOBR_RS08260 in Desulfovibrio oxyclinae DSM 11498

Align Branched-chain amino acid ABC transporter,substrate-binding periplasmic component (characterized, see rationale)
to candidate WP_018124026.1 B149_RS0104760 branched-chain amino acid ABC transporter substrate-binding protein

Query= uniprot:G8ALJ3
         (366 letters)



>NCBI__GCF_000375485.1:WP_018124026.1
          Length = 380

 Score =  191 bits (486), Expect = 2e-53
 Identities = 111/345 (32%), Positives = 169/345 (48%), Gaps = 6/345 (1%)

Query: 25  IAVATAGPITGQYATFGEQMKKGIEQAVADINAAGGVLGQKLKLEVGDDACDPKQAVAVA 84
           + +  AG  +G  A++G       +     INA GGVLG ++++   DD C P+ A   A
Sbjct: 36  LVLGVAGAHSGDLASYGLPTVNAAKLVAKKINAEGGVLGMQVEVMAQDDQCKPEMATNAA 95

Query: 85  NQLAKAGVKFVAGHFCSGSSIPASQVYAEEGVLQISPASTNPKLTEQ-NLKNVFRVCGRD 143
            +L    VK V GH CSG++  A ++Y +  ++ +SP++TNP LT+  N  N FR    D
Sbjct: 96  TKLLSEDVKIVLGHICSGATKAALEIYKDGNIVCMSPSATNPPLTQSGNYPNFFRTIASD 155

Query: 144 DQQGQIAGKYLLENYKGKNVAILHDKSAYGKGLADETQKAL-NAGGQKEKIYEAYTAGEK 202
           D Q  +   +  +    KN+A++HDK  YGKG A   Q+ +    G    ++E  T G  
Sbjct: 156 DAQASLEVDF-AKKLGLKNIAVIHDKGDYGKGFASFCQQFIEEEDGMSVALFEGVTPGAV 214

Query: 203 DYSALVSKLKQEAVDVVYVGGYHTEAGLLARQMKDQGLNAPIVSGDALVTNEYWAITGPA 262
           DYSA+V K+K    D V  GGYH EA  +   M+ + +  P +S D +    +  + G  
Sbjct: 215 DYSAVVQKIKNSGADGVIFGGYHPEASKIVTSMRKKNIEVPFLSDDGVKDETFIKVAGEY 274

Query: 263 GENTMMTFGPDPREMP--EAKEAVEKFRKAGYEPEGYTLYTYAALQIWAEAAKQANSTDS 320
            E    T   D    P     E+  K  + G +P  +    YAA Q    A ++A + D 
Sbjct: 275 AEGVYATGPRDISGNPLYSVAESAHK-EEFGSDPGAFYYQAYAAAQALLNAVEKAGAVDY 333

Query: 321 AKIADVLRKNSYNTVIGKIGFDAKGDVTSPAYVWYRWNNGQYAQV 365
            KI + LR     T +GKI FD +GD     +  Y+  +GQY ++
Sbjct: 334 DKIVEALRTEYVETPLGKIKFDDRGDAEGVGFSMYQVKDGQYVEI 378


Lambda     K      H
   0.312    0.129    0.366 

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: 359
Number of extensions: 25
Number of successful extensions: 4
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: 366
Length of database: 380
Length adjustment: 30
Effective length of query: 336
Effective length of database: 350
Effective search space:   117600
Effective search space used:   117600
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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