GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Hyphomicrobium sulfonivorans WDL6

Align ABC transporter for D-Glucose-6-Phosphate, ATPase component (characterized)
to candidate WP_083509566.1 APY04_RS07015 ABC transporter ATP-binding protein

Query= reanno::WCS417:GFF4321
         (386 letters)



>NCBI__GCF_001541235.1:WP_083509566.1
          Length = 392

 Score =  183 bits (465), Expect = 6e-51
 Identities = 120/365 (32%), Positives = 187/365 (51%), Gaps = 27/365 (7%)

Query: 2   ATLELRNVNKTYGAGLPDTLKNIELSIKEGEFLILVGPSGCGKSTLMNCIAGLETITGGA 61
           A L   +V + +G      L  + L I  GE + L+GPSGCGK+TL+   AG+E  TGG 
Sbjct: 44  ACLTFEDVRRNFGT--TQALAGVSLEIDRGEVVCLLGPSGCGKTTLLRIAAGIERPTGGR 101

Query: 62  IMIGDQDVSGMS----PKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKMPQADIDAEVA 117
           ++I   +V+G S    P+ R + ++FQ +AL+P +++  N+ FGLK   +P+A+   E  
Sbjct: 102 VLINGHEVAGPSSFVVPEKRSVGLMFQDFALFPHLTIAGNVAFGLK--SLPRAEAKREAL 159

Query: 118 RVAKLLQIEHLLNRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTE 177
              K + +EH+ +  P  LSGGQQQRVA+ RAL  RP + L DEP S LD +LR  M+ E
Sbjct: 160 AALKRVGLEHMADEYPHVLSGGQQQRVALARALVPRPAVMLMDEPFSGLDVQLRDAMQEE 219

Query: 178 MKLMHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKEIYNNPANQFVASFIG 237
              + +    T + VTH+  EAM +GD++ VM+ G + Q G  + +Y+ PA+ FVA    
Sbjct: 220 TLSLLRETGATAMVVTHNPEEAMRIGDRIVVMRAGGLIQQGQAEALYHQPADLFVARLFS 279

Query: 238 SPPMNFVPLRLQRKDGRLVALLDSGQARCELALNTTEAGLEDRD-VILGLRPEQIMLAAG 296
              +N V  R+             G+    +   +  AGL+  D V +G+R   I L+  
Sbjct: 280 E--INEVAYRVGA----------DGKIDTPIGKLSPPAGLQAHDAVTIGVRERDIRLS-- 325

Query: 297 EGDSASSIRAEVQVTEPTGPDTLVFVQLN--DTKVCCRLAPDVAPQVGETLTLQFDPSKV 354
             D+   +   V   +  G    + V +   D  +  R+      + G  +  Q DP + 
Sbjct: 326 --DNGEGLSGRVLDAKFLGDVVRLEVGIEGFDQPLKVRVRESAGFRQGHDVRAQIDPERA 383

Query: 355 LLFDA 359
           L+F A
Sbjct: 384 LVFAA 388


Lambda     K      H
   0.318    0.135    0.382 

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: 382
Number of extensions: 16
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: 386
Length of database: 392
Length adjustment: 30
Effective length of query: 356
Effective length of database: 362
Effective search space:   128872
Effective search space used:   128872
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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