GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21106 in Rhodobacter viridis JA737

Align ABC transporter for L-Fucose, ATPase component (characterized)
to candidate WP_110805339.1 C8J30_RS08100 ABC transporter ATP-binding protein

Query= reanno::Smeli:SM_b21106
         (365 letters)



>NCBI__GCF_003217355.1:WP_110805339.1
          Length = 348

 Score =  260 bits (665), Expect = 3e-74
 Identities = 146/333 (43%), Positives = 207/333 (62%), Gaps = 22/333 (6%)

Query: 1   MAPVTLKKLVKRYGALEVVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGAI 60
           M+ ++L  L K +G L VV   +L V+  EFI+L+GPSGCGK+T LRM+AG E  + GAI
Sbjct: 1   MSYLSLTHLEKSFGTLRVVKDFNLTVEKGEFISLLGPSGCGKTTVLRMVAGFELPTSGAI 60

Query: 61  EIGGRKVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAAI 120
            I G++V DL P  RNI MVFQ+YAL+P++TVA+N+GF LK+ G P   I  RV E  ++
Sbjct: 61  TIAGKEVTDLKPNQRNIGMVFQAYALFPNLTVAQNVGFGLKVKGTPKAAIDKRVEEMLSL 120

Query: 121 LDLAHLLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKLH 180
           + L  L  R P QLSGGQ+QRVA+ RA+  +P V L DEPLS LDAK+R  +R EI+ + 
Sbjct: 121 IGLPDLGNRYPFQLSGGQQQRVALARALAPKPSVLLLDEPLSALDAKVRVSLRNEIRAIQ 180

Query: 181 ARMQATMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGS-PPM 239
             +  T I+VTHDQ EA+++SDR+V+M +G  +QVGTP D++ RP+T+FVA F+G+   +
Sbjct: 181 RELGITTIFVTHDQEEALSMSDRVVVMHEGIADQVGTPFDIYNRPSTRFVASFVGTLNTL 240

Query: 240 NMEEAVLTDGKL-----AFASGATLPLPPRFRSLVREGQKVTFGLRPDDVYPSGHGLHAG 294
           N++     +G++       A G +LP  P           VT GLRP+ V   G G H  
Sbjct: 241 NVQVLDAANGRVKLGATEIALGRSLPSGP-----------VTLGLRPEAV-TLGQGNHDT 288

Query: 295 DADA-VHEIEL---PVTITEPLGNETLVFTQFN 323
              A + E++     + +   L  + + F  FN
Sbjct: 289 RLSATIREVDFLGSVIRLRADLAGQPIAFDTFN 321


Lambda     K      H
   0.320    0.137    0.397 

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: 339
Number of extensions: 12
Number of successful extensions: 1
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: 365
Length of database: 348
Length adjustment: 29
Effective length of query: 336
Effective length of database: 319
Effective search space:   107184
Effective search space used:   107184
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: 49 (23.5 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