GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Marinobacter adhaerens HP15

Align Maltose-transporting ATPase (EC 3.6.3.19) (characterized)
to candidate GFF2209 HP15_2163 sugar ABC transporter, ATP-binding protein

Query= reanno::psRCH2:GFF857
         (371 letters)



>FitnessBrowser__Marino:GFF2209
          Length = 366

 Score =  225 bits (573), Expect = 2e-63
 Identities = 134/364 (36%), Positives = 204/364 (56%), Gaps = 30/364 (8%)

Query: 1   MASVTLRDICKSYDGTPI------TRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLED 54
           MA + L+ +  SY   P        R +D     G     +GPSGCGKST+L +I+GL  
Sbjct: 1   MAEIQLKSLAHSYSDMPTGPDDYAIRQLDHVWHKGGAYALLGPSGCGKSTMLNIISGLVQ 60

Query: 55  ITSGDLLIDNQRVNDLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRV 114
            + GD+L D +RVN+L P+DR++  VFQ   +Y  MTV +N+AF LK   V   +IK RV
Sbjct: 61  PSEGDVLFDGKRVNELSPRDRNIAQVFQFPVIYDSMTVYDNLAFPLKNNKVPASKIKARV 120

Query: 115 EAVAEILQLDKLLERKPKDLSGGQRQRVAIGRTMVREP-KVFLFDEPLSNLDAFLRVQMR 173
             +AE+L+++  L +K K+L+  ++Q+V++GR +VRE     LFDEPL+ +D  L+ ++R
Sbjct: 121 HEIAEVLEIEDKLYKKAKNLTADEKQKVSMGRGLVREDVSAILFDEPLTVIDPQLKWKLR 180

Query: 174 IEIARLHQRIRSTMIYVTHDQVEAMTLADKIVVLNAGEIAQVGQPLHLYHYPKNRFVAGF 233
            ++ ++H++   TM+YVTHDQ+EA T ADKI V+  G+I Q G P  L+  P + FV  F
Sbjct: 181 RKLKQIHEQFDITMVYVTHDQLEASTFADKIAVMYGGQIVQFGTPTELFEQPNHTFVGFF 240

Query: 234 LGSPQMNFVEV----RAISASPETVTIELPSGYPLTLPVDGSAVSPGDPLTLGIRPEHFV 289
           +GSP MN +EV    R +      V++E       +  VD    +    + +GIRPE   
Sbjct: 241 IGSPGMNLIEVQRCPRGVCFGSTVVSLE-------SWQVDVLQRTRSTNIKIGIRPEFVE 293

Query: 290 MPDEA-DFTFHGQITVAERLGQYNLLYLTLERLQDVITLCVDGNLRVTEGETFAAGLKAD 348
           +   A D TF  ++   E LG Y ++ + L+             ++V + E FAA +   
Sbjct: 294 VSSVASDDTFEAEVLDVEDLGTYKIVTVQLDH----------EKMKVRQSEEFAASI-GS 342

Query: 349 KCHL 352
           K HL
Sbjct: 343 KVHL 346


Lambda     K      H
   0.322    0.139    0.405 

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: 305
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: 371
Length of database: 366
Length adjustment: 30
Effective length of query: 341
Effective length of database: 336
Effective search space:   114576
Effective search space used:   114576
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 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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