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 GFF3011 HP15_2955 ATP-binding component of ABC transporter

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



>FitnessBrowser__Marino:GFF3011
          Length = 372

 Score =  306 bits (783), Expect = 8e-88
 Identities = 170/351 (48%), Positives = 228/351 (64%), Gaps = 14/351 (3%)

Query: 1   MASVTLRDICKSYDGTP--ITRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLEDITSG 58
           M+ + LR I K+Y G      + ID+DI  GEF++ VGPSGCGKSTL+  IAGLE IT G
Sbjct: 1   MSQLELRSIRKTYPGVAEETLKGIDIDIASGEFLILVGPSGCGKSTLMNTIAGLETITDG 60

Query: 59  DLLIDNQRVNDLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRVEAVA 118
            +++D + ++ + PKDR + MVFQSYALYP M+V EN+AFGLK+  + K EI + VE VA
Sbjct: 61  SIVLDGKDISTMEPKDRDIAMVFQSYALYPTMSVRENIAFGLKIRGLPKHEIDQEVERVA 120

Query: 119 EILQLDKLLERKPKDLSGGQRQRVAIGRTMVREPKVFLFDEPLSNLDAFLRVQMRIEIAR 178
           ++LQ+  L+ +KP +LSGGQ+QRVA+GR + R P+++LFDEPLSNLDA LRV+MR EI +
Sbjct: 121 DLLQISPLMNKKPANLSGGQQQRVAMGRALARRPRIYLFDEPLSNLDAKLRVEMRTEIKK 180

Query: 179 LHQRIRSTMIYVTHDQVEAMTLADKIVVLNAGEIAQVGQPLHLYHYPKNRFVAGFLGSPQ 238
           LHQR+++T++YVTHDQ+EAMTLAD+I VL  GE+ Q+G P  +Y  P+N FVAGF+GSP 
Sbjct: 181 LHQRLKTTIVYVTHDQIEAMTLADRIAVLKDGELQQLGTPKEVYDRPENLFVAGFMGSPA 240

Query: 239 MNFVEVRAISASPE-TVTIELPSGYPLTLPV-DGSAVSPGDPLTLGIRPEHFVMP----D 292
           M+FV V            +    G  + LPV +  A   G  + LGIRPEH   P    +
Sbjct: 241 MSFVPVTVEQGEGGLQAEVRGNDGRSVKLPVPEFLADRVGKKVILGIRPEHITQPQDQKN 300

Query: 293 EADFTFHGQIT--VAERLGQYNLLYLTLERLQDVITLC-VDGNLRVTEGET 340
           +      G+ T  V E  G      + L +L D    C +D    VT GET
Sbjct: 301 DQTLVAKGEFTIEVTEPTGPD---VIALIQLNDTNVHCRIDPEHPVTWGET 348


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: 442
Number of extensions: 21
Number of successful extensions: 2
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: 372
Length adjustment: 30
Effective length of query: 341
Effective length of database: 342
Effective search space:   116622
Effective search space used:   116622
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