GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Marinobacter adhaerens HP15

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate GFF4122 HP15_4062 spermidine/putrescine ABC transporter, ATP-binding protein

Query= reanno::Dino:3607124
         (338 letters)



>FitnessBrowser__Marino:GFF4122
          Length = 373

 Score =  233 bits (595), Expect = 4e-66
 Identities = 129/330 (39%), Positives = 197/330 (59%), Gaps = 23/330 (6%)

Query: 4   IKIDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRIEIG 63
           + +  ++K +G    L  ++L+I DGEF+  +GPSGCGK+TLLR +AG E    G I + 
Sbjct: 6   LSLSNLSKQFGGKTVLDGLDLEIYDGEFITLLGPSGCGKTTLLRLMAGFEHPDEGTITLA 65

Query: 64  GRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAARVLQL 123
           G ++T   P +R L  VFQ YAL+PHM+V +N+ +G+K+     D  ++R+ EA  ++QL
Sbjct: 66  GENLTHTAPENRPLNTVFQHYALFPHMSVFDNVAYGLKMEKRPKDEIRQRVDEALAMVQL 125

Query: 124 EDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEGLHKQL 183
           +D+  RKP QLSGGQ+QRVAI RA+VK P + L DEPLS LD KLR  M+VEL+ L ++L
Sbjct: 126 QDFARRKPHQLSGGQQQRVAIARAVVKRPRLLLLDEPLSALDYKLRRTMQVELKRLQREL 185

Query: 184 GATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPAMNVFS 243
           G T ++VTHDQ EA++M+D++VVL  G ++Q+G+P ++Y +P + F A F+G    N F 
Sbjct: 186 GITFVFVTHDQEEALSMSDRVVVLKDGLVQQLGTPREVYERPANLFTARFVGE--TNFFP 243

Query: 244 SDV-GLQDISLDA-------------------SAAFVGCRPEHIEIV-PDGDGHIAATVH 282
             V  +QD S+                      +  V  RPE I ++ PD +  +A  + 
Sbjct: 244 GTVESVQDGSIKVDVFGLKRTLRRPDFPVQAEQSLHVLLRPEDIRVLEPDDENGVAGKIV 303

Query: 283 VKERLGGESLLYLGLKGGGQIVARVGGDDE 312
            +   G      + L  G +++A    D++
Sbjct: 304 ERNYKGSTLDSVIHLADGTEVLASEFFDED 333


Lambda     K      H
   0.320    0.139    0.396 

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: 330
Number of extensions: 15
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: 338
Length of database: 373
Length adjustment: 29
Effective length of query: 309
Effective length of database: 344
Effective search space:   106296
Effective search space used:   106296
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 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