GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21216 in Cupriavidus basilensis 4G11

Align ABC transporter for D-Glucosamine, ATPase component (characterized)
to candidate RR42_RS37305 RR42_RS37305 sulfate ABC transporter ATP-binding protein

Query= reanno::Smeli:SM_b21216
         (360 letters)



>FitnessBrowser__Cup4G11:RR42_RS37305
          Length = 366

 Score =  223 bits (568), Expect = 6e-63
 Identities = 130/301 (43%), Positives = 180/301 (59%), Gaps = 8/301 (2%)

Query: 4   LEIRNIRKRYGEV---ETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDI 60
           L +  + KR+G     + L G+ +++  GE L LLG SGCGK+TLL IIAGL     G I
Sbjct: 13  LAVEQVGKRFGGAGGFQALDGVSLSVAQGELLCLLGPSGCGKTTLLRIIAGLEREDTGRI 72

Query: 61  LIGERSVLGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRDTARL 120
             G R + G+ P+ RD  ++FQSYAL+PNLSVARN+ +GL+ R + +A  +  V +   L
Sbjct: 73  HAGGRELTGLPPQARDYGILFQSYALFPNLSVARNVAYGLQGRGMGRAHREARVAEMLSL 132

Query: 121 LQIENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTELKRLH 180
           + +     + P QLSGGQ+QRVA+ RAL   P + L DEP+S LDA++R  +R EL++L 
Sbjct: 133 VGLAGSERKFPGQLSGGQQQRVALARALAPAPSLLLLDEPMSALDARVREHLRLELRQLQ 192

Query: 181 QMLRTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGSPPMN 240
           + L  T V VTHDQ EAM +A RIAVM  GRI Q+  P E+Y+RPA+ +VA F+G    N
Sbjct: 193 RRLNVTTVMVTHDQDEAMAMADRIAVMEGGRIAQVGTPGEIYERPASAFVAEFIGQ--AN 250

Query: 241 ILDAEMTANGLKIEGCEEVLPLPAAFNGAAWAGRRVKVGIRPEALRL-AAGSEAQRLTAS 299
            LD  ++       G  ++   PA  +  A    R  +  RPEA+RL     E  RL A 
Sbjct: 251 WLDGRLSGRDTFSVGELDLAVSPARASEVADGAAR--LCCRPEAIRLHPVEGEPNRLLAR 308

Query: 300 V 300
           +
Sbjct: 309 I 309


Lambda     K      H
   0.320    0.136    0.385 

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: 348
Number of extensions: 17
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: 360
Length of database: 366
Length adjustment: 29
Effective length of query: 331
Effective length of database: 337
Effective search space:   111547
Effective search space used:   111547
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