GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Methanosarcina acetivorans C2A

Align GtsD (GLcK), component of Glucose porter, GtsABCD (characterized)
to candidate WP_011022261.1 MA_RS11835 ABC transporter ATP-binding protein

Query= TCDB::Q88P35
         (384 letters)



>NCBI__GCF_000007345.1:WP_011022261.1
          Length = 383

 Score =  178 bits (451), Expect = 3e-49
 Identities = 122/371 (32%), Positives = 190/371 (51%), Gaps = 27/371 (7%)

Query: 9   VNKTYGSGLPDTLKDIQLSIKDGEFLILVGPSGCGKSTLMNCIAGLEQITGGAILI---- 64
           +N+   +G   TL D+   + D E ++L GPSG GK+TL  CI+G+ Q   G I +    
Sbjct: 18  INRKRSTGKAFTL-DVSFEM-DNELVVLFGPSGSGKTTLFKCISGITQPDNGKITVGSKI 75

Query: 65  --DEQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKLPQAAIDEEVARVAKL 122
             D+     +  + R++  VFQ+Y L+P M+VR+NIE GLK  K  +   +  V  +  L
Sbjct: 76  YYDKDKKINLPIQKRNLGYVFQNYTLFPHMNVRKNIECGLK--KWEKEDREVRVMEMLNL 133

Query: 123 LQIEHLLARKPAQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKLMH 182
           L IE L    P+QLSGGQ+QRVA+ RALA +P++ L DEP S LD  LR+E+  ++K + 
Sbjct: 134 LHIEELETHYPSQLSGGQKQRVALARALAPKPELLLLDEPFSALDRVLRIELAEKLKKLQ 193

Query: 183 QRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPQQIYNDPANQFVASFIGSPPMN 242
           +R+     ++TH   EA  L D++ ++  G +QQFG P++I+  P N  VA   G   + 
Sbjct: 194 KRIGIPLAFITHSLDEAFVLADRILILYRGEVQQFGAPEEIFYHPRNLHVAELAGLSNI- 252

Query: 243 FIPVRLARQDGRLLALLDSGQARCELPLGEAADAL------EGREIILGIRPEQIAL--- 293
           F   R+  Q  +L+   ++G  R  L  GE   A+      EG ++  GI PE I L   
Sbjct: 253 FDDARVEEQVEKLVEGNNAGPKRTVLKSGEMRIAVNPLNLKEGDKVSWGIHPENITLLLP 312

Query: 294 -GAADGNGLPAIRAEVQVTEPTGPDLLVFVTLNQ------TKVCCRLAPDVACRVGDTLN 346
              ++        A V      GP   + + L +       +V  + A  +    GD   
Sbjct: 313 NSGSEDKDENVYSAYVHSITGKGPKKRIVLKLARHEKSLNAEVPAQFADALNLNTGDLCL 372

Query: 347 LQFDPARVLLF 357
           ++ D ++V+ F
Sbjct: 373 VKMDMSKVVAF 383


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: 355
Number of extensions: 15
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: 383
Length adjustment: 30
Effective length of query: 354
Effective length of database: 353
Effective search space:   124962
Effective search space used:   124962
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 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