GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglA in Jannaschia aquimarina GSW-M26

Align Monosaccharide-transporting ATPase, component of Glucose porter. Also bind xylose (Boucher and Noll 2011). Induced by glucose (Frock et al. 2012). Directly regulated by glucose-responsive regulator GluR (characterized)
to candidate WP_043920019.1 jaqu_RS16085 sugar ABC transporter ATP-binding protein

Query= TCDB::G4FGN3
         (494 letters)



>NCBI__GCF_000877395.1:WP_043920019.1
          Length = 498

 Score =  340 bits (872), Expect = 7e-98
 Identities = 181/484 (37%), Positives = 294/484 (60%), Gaps = 3/484 (0%)

Query: 3   PILEVKSIHKRFPGVHALKGVSMEFYPGEVHAIVGENGAGKSTLMKIIAGVYQPDEGEII 62
           P++ ++ + KR+  + AL  V +    GE   + GENG+GKSTL+K++ GV +P  G I+
Sbjct: 7   PLVTLEGVTKRYAAITALSEVDLTIRAGEAVCLAGENGSGKSTLIKVLVGVERPSAGRIL 66

Query: 63  YEGRGVRWNHPSEAINAGIVTVFQELSVMDNLSVAENIFMGDEEKRGIFIDYKKMYREAE 122
           ++G       P+ A  AG+  +FQ+ S+  NLSVAENI M  E   G  + +++  RE  
Sbjct: 67  FDGVPQTRLTPTAATRAGMQVIFQDFSLFPNLSVAENIAMTAERATGARLVHRRRARERA 126

Query: 123 KFMKEEFGIEIDPEEKLGKYSIAIQQMVEIARAVYKKAKVLILDEPTSSLTQKETEKLFE 182
           + + +  G+++D + ++ +  +A +Q+V I RA+   A+++I+DEPT++LT++E  +L +
Sbjct: 127 REVLDRIGVDLDLDARVERLPVAHKQLVAICRALAADARLIIMDEPTTALTEREVARLLD 186

Query: 183 VVKSLKEKGVAIIFISHRLEEIFEICDKVSVLRDGEYIGTDSIENLTKEKIVEMMVGRKL 242
           +++ LK  GVA++F+SH+L E+ E+C+ V VLR+GE +     E      +   M GR +
Sbjct: 187 LIRRLKADGVAVLFVSHKLAEVLEVCEHVVVLRNGEKVADGPAETFDAASLTRAMTGRDV 246

Query: 243 EKFYIKEAHEPGEVVLEVKNLSGE-RFENVSFSLRRGEILGFAGLVGAGRTELMETIFGF 301
            +   +        +L+V+NL+ +  F +VS +LR GE+LG AGL+G+GRT L + +FG 
Sbjct: 247 AETPPEPLDPSASDLLKVENLTKDGAFRDVSLTLRAGEVLGVAGLLGSGRTSLAKALFGL 306

Query: 302 RPKRGGEIYIEGKRVEINHPLDAIEQGIGLVPEDRKKLGLILIMSIMHNVSLPSLDRIKK 361
                G + ++G  V +  P+ A   GIG VPEDR   GL L  SI  N+++  L+    
Sbjct: 307 ATPDSGRVTLDGTDVPLGDPIAAAGAGIGYVPEDRLTEGLFLEQSIARNIAVGRLEAHAS 366

Query: 362 GPFISFKRE-KELADWAIKTFDIRPAYPDRKVLYLSGGNQQKVVLAKWLALKPKILILDE 420
           G  ++ +   +E A+W +K   ++   P   V  LSGGNQQ+VVLA+W+A +P++LIL+ 
Sbjct: 367 GGVLNLRDLWEEAAEW-LKRLSVKAPDPQAPVRSLSGGNQQRVVLARWMARQPRVLILNG 425

Query: 421 PTRGIDVGAKAEIYRIMSQLAKEGVGVIMISSELPEVLQMSDRIAVMSFGKLAGIIDAKE 480
           P+ G+DVG+KAEI+ I+S LA  G+GVI+IS +LPE+L    RI VM  G +   +   E
Sbjct: 426 PSVGVDVGSKAEIHAIISDLAARGLGVIVISDDLPELLGTCHRILVMKAGVITDEVAGGE 485

Query: 481 ASQE 484
              E
Sbjct: 486 GITE 489


Lambda     K      H
   0.318    0.138    0.385 

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: 579
Number of extensions: 27
Number of successful extensions: 6
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: 494
Length of database: 498
Length adjustment: 34
Effective length of query: 460
Effective length of database: 464
Effective search space:   213440
Effective search space used:   213440
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: 52 (24.6 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