GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Halococcus hamelinensis 100A6

Align GtsD (GLcK), component of Glucose porter, GtsABCD (characterized)
to candidate WP_007692556.1 C447_RS07635 ABC transporter ATP-binding protein

Query= TCDB::Q88P35
         (384 letters)



>NCBI__GCF_000336675.1:WP_007692556.1
          Length = 362

 Score =  291 bits (746), Expect = 2e-83
 Identities = 164/368 (44%), Positives = 224/368 (60%), Gaps = 18/368 (4%)

Query: 3   TLELRNVNKTYGSGLPDTLKDIQLSIKDGEFLILVGPSGCGKSTLMNCIAGLEQITGGAI 62
           T+EL N++K +GS +   + D+ L+I++GEFLILVGPSGCGK+T +  IAGLE+ + G I
Sbjct: 2   TVELSNISKRFGSIV--AVDDVSLTIENGEFLILVGPSGCGKTTTLRMIAGLEKPSSGRI 59

Query: 63  LIDEQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKLPQAAIDEEVARVAKL 122
             D  DV+  SP+ R IA VFQ+YALYP M+ R+N+ F L+ + +P   + + V   A  
Sbjct: 60  YFDGDDVTQFSPQQRHIAFVFQNYALYPHMTTRKNMSFALEDQDIPSDEVAQRVTSTADK 119

Query: 123 LQIEHLLARKPAQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKLMH 182
           L I   L ++P +LSGGQQQRVA+GR++ R P ++L DEPLSNLDAKLR  MR E++ +H
Sbjct: 120 LGITDQLDQRPGELSGGQQQRVALGRSIVRNPSVFLLDEPLSNLDAKLRTNMRAELQELH 179

Query: 183 QRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPQQIYNDPANQFVASFIGSPPMN 242
           Q L+TT VYVTHDQ EAMT+GD++AVM +G IQQ   P + YN PAN+FVA FIGSP MN
Sbjct: 180 QDLETTMVYVTHDQEEAMTMGDRIAVMDEGTIQQVAPPNEAYNQPANRFVAGFIGSPSMN 239

Query: 243 FIPVRLARQDGRLLALLDSGQARCELPLGEAADALEGREIILGIRPEQIAL-GAADGNGL 301
           F             A LD G+ R         D + G    LGIRPE +++   A G   
Sbjct: 240 FFD-----------ASLDDGRVRAGPFTLPTPDRVSGPLSELGIRPEDVSVTPTATGED- 287

Query: 302 PAIRAEVQVTEPTGPDLLVFVTLNQTKVCCRLAPDVACRVGDTLNLQFDPARVLLFDAAN 361
             + A V V E  G   ++++ ++   +       V    GD + +  D  RV LFD   
Sbjct: 288 --VSATVTVFEQVGSSNIIYLEIDGETMIAETDASVQLAPGDDVGVSLDTERVHLFD-RG 344

Query: 362 GERLHLAS 369
           G+ +H  S
Sbjct: 345 GDAVHSPS 352


Lambda     K      H
   0.320    0.137    0.391 

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: 379
Number of extensions: 13
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: 384
Length of database: 362
Length adjustment: 30
Effective length of query: 354
Effective length of database: 332
Effective search space:   117528
Effective search space used:   117528
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: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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:

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