GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PfGW456L13_1897 in Rhodobacter viridis JA737

Align ABC transporter for D-Galactose and D-Glucose, ATPase component (characterized)
to candidate WP_110805339.1 C8J30_RS08100 ABC transporter ATP-binding protein

Query= reanno::pseudo13_GW456_L13:PfGW456L13_1897
         (386 letters)



>NCBI__GCF_003217355.1:WP_110805339.1
          Length = 348

 Score =  239 bits (609), Expect = 1e-67
 Identities = 143/363 (39%), Positives = 216/363 (59%), Gaps = 25/363 (6%)

Query: 1   MATLELRNVNKTYGPGLPDTLKNIELKIDDGEFLILVGPSGCGKSTLMNCIAGLETISGG 60
           M+ L L ++ K++G      +K+  L ++ GEF+ L+GPSGCGK+T++  +AG E  + G
Sbjct: 1   MSYLSLTHLEKSFGT--LRVVKDFNLTVEKGEFISLLGPSGCGKTTVLRMVAGFELPTSG 58

Query: 61  AILVDDADISGMSPKDRDIAMVFQSYALYPTMSVRDNIAFGLKIRKMPTAEIDEEVARVS 120
           AI +   +++ + P  R+I MVFQ+YAL+P ++V  N+ FGLK++  P A ID+ V  + 
Sbjct: 59  AITIAGKEVTDLKPNQRNIGMVFQAYALFPNLTVAQNVGFGLKVKGTPKAAIDKRVEEML 118

Query: 121 KLLQIEHLLSRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180
            L+ +  L +R P QLSGGQQQRVA+ RALA +P + L DEPLS LDAK+RV +R E++ 
Sbjct: 119 SLIGLPDLGNRYPFQLSGGQQQRVALARALAPKPSVLLLDEPLSALDAKVRVSLRNEIRA 178

Query: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKDIYNNPANLFVASFIGSPP 240
           + + L  TT++VTHDQ EA+++ D+V VM +GI  Q GTP DIYN P+  FVASF+G+  
Sbjct: 179 IQRELGITTIFVTHDQEEALSMSDRVVVMHEGIADQVGTPFDIYNRPSTRFVASFVGT-- 236

Query: 241 MNFIPLR-LQRKDGRLLALLDSGQARCELPLGMQDAGLEDREVILGIRPEQIILANGEAN 299
           +N + ++ L   +GR+           E+ LG     L    V LG+RPE + L  G+ N
Sbjct: 237 LNTLNVQVLDAANGRVKL------GATEIALG---RSLPSGPVTLGLRPEAVTL--GQGN 285

Query: 300 GLPTIRAEVQVTEPTGPDTLVFVNLN------DTKVCCRLAPDVAPAVGETLTLQFDPAK 353
               + A ++  +  G    +  +L       DT      AP   P VG  +TL  + A 
Sbjct: 286 HDTRLSATIREVDFLGSVIRLRADLAGQPIAFDTFNNSHAAP---PEVGTEVTLGLNAAD 342

Query: 354 VLL 356
           +L+
Sbjct: 343 LLV 345


Lambda     K      H
   0.319    0.138    0.393 

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: 333
Number of extensions: 7
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: 386
Length of database: 348
Length adjustment: 30
Effective length of query: 356
Effective length of database: 318
Effective search space:   113208
Effective search space used:   113208
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 (21.7 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