GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Phyllobacterium brassicacearum STM 196

Align ABC transporter for Glycerol, ATPase component 1 (characterized)
to candidate WP_106713056.1 CU102_RS21035 ABC transporter ATP-binding protein

Query= reanno::acidovorax_3H11:Ac3H11_791
         (363 letters)



>NCBI__GCF_003010955.1:WP_106713056.1
          Length = 355

 Score =  200 bits (509), Expect = 4e-56
 Identities = 122/352 (34%), Positives = 189/352 (53%), Gaps = 11/352 (3%)

Query: 3   LALDSISKKVGAQTWLYDMSLALQSGAVTVLLGATQAGKTSLMRIMAGLDAPTAGRVTVD 62
           + L +++K  G+   L+D+SL +      V +G +  GK++L+R++AGLD P+ G +T+D
Sbjct: 4   IKLTNVAKSFGSVDVLHDISLEIADSEFVVFVGPSGCGKSTLLRMIAGLDRPSRGELTID 63

Query: 63  GKDVTGMPVRDRNVAMVYQQFINYPSMKVAANIASPLK--LRGEKNIDARVREIASRLHI 120
           GK V  +P  DR +AMV+Q +  YP M V  N+A  L+     +  I  R+ E A  L I
Sbjct: 64  GKLVNNVPAADRGLAMVFQSYALYPHMSVRQNLAFGLENTKMPKAEIVERIAEAARMLEI 123

Query: 121 DMFLDRYPAELSGGQQQRVALARALAKGAPLMLLDEPLVNLDYKLREELREELTQLFAAG 180
           + +L+R P +LSGGQ+QRVA+ RA+ +     LLDEPL NLD +LR   R EL  L A  
Sbjct: 124 EPYLERRPGQLSGGQRQRVAIGRAIVRRPVAFLLDEPLSNLDAELRGSTRAELAALHARL 183

Query: 181 QSTVVYATTEPGEALLLGGYTAVLDEGQLLQYGPTAEVFHAPNSLRVARAFSDPPMNLMA 240
            +T++Y T +  EA+ L     VL  G++ Q G   E++++P +  VA     P MN + 
Sbjct: 184 SATMIYVTHDQVEAMTLADRIVVLRAGRVEQVGTPLELYNSPANRFVAGFIGSPHMNFLD 243

Query: 241 ASATAQG-----VRLQGGAELTLPLPQGAATAAGLTVGVRASALRVHARPGDVSVAGVVE 295
            +  + G     V L GG  + +P+  G A  A +T+GVR   + +  + G   +   ++
Sbjct: 244 GTIESLGPSKAVVALTGGHRVEVPV-DGTAAGARVTLGVRPQHISIGDKQG---IPAEIK 299

Query: 296 LAEISGSDTFVHASTPWGDLVAQLTGVHYFELGTAITLHLDPAQAYVFGADG 347
           L E  GS+T +HA      ++    G H    G  I L L  A  ++F   G
Sbjct: 300 LVEALGSETVLHADVAGQKVLVVAPGQHDLMAGAGIHLSLSAAPLHIFNEQG 351


Lambda     K      H
   0.318    0.133    0.375 

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: 300
Number of extensions: 18
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: 363
Length of database: 355
Length adjustment: 29
Effective length of query: 334
Effective length of database: 326
Effective search space:   108884
Effective search space used:   108884
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 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