GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21216 in Phaeobacter inhibens BS107

Align ABC transporter for D-Glucosamine, ATPase component (characterized)
to candidate GFF1915 PGA1_c19470 ABC transporter, ATP-binding protein

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



>FitnessBrowser__Phaeo:GFF1915
          Length = 363

 Score =  326 bits (835), Expect = 7e-94
 Identities = 182/354 (51%), Positives = 234/354 (66%), Gaps = 5/354 (1%)

Query: 2   SALEIRNIRKRYGEVETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDIL 61
           S +  R++  R+G VE LK +++ ++ GEFLVLLG+SGCGKSTLLN IAGL E + G I 
Sbjct: 11  SHVSARDLSVRFGAVEVLKSLNLDIQKGEFLVLLGASGCGKSTLLNTIAGLQEATEGQIW 70

Query: 62  IGERSVLGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRDTARLL 121
           I + +V    PKDR +AMVFQSYALYP ++V  N+ FGL M +VP+AE DK V + AR+L
Sbjct: 71  INDENVTWREPKDRGLAMVFQSYALYPKMTVRGNLAFGLRMNKVPKAEADKLVDEAARVL 130

Query: 122 QIENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTELKRLHQ 181
           Q+E LLDR+P +LSGGQRQRVAIGRALVR   VFLFDEPLSNLDAKLR E+R ELKRLHQ
Sbjct: 131 QLEELLDRRPGELSGGQRQRVAIGRALVRKVDVFLFDEPLSNLDAKLRAELRVELKRLHQ 190

Query: 182 MLRTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGSPPMNI 241
            L  T++YVTHDQ+EA+TLA RIAVM+DG ++QL +P+E+Y RPA  YVA FVG P MN 
Sbjct: 191 ELGATMIYVTHDQVEALTLADRIAVMKDGVVQQLDSPEEIYRRPANRYVAQFVGLPSMNF 250

Query: 242 LDAEMTANG-LKIEGCEEVLPLPAAFNGAAWAGRRVKVGIRPEALRLAAGSEAQRLTASV 300
           ++  +T +G ++ E  E  L      +  A  G  V++GIRPE +  A    A      V
Sbjct: 251 VNGVVTESGAIQTEDFELALDQCNLASTPA-PGTEVEIGIRPEHVHPA---NAGGFMLDV 306

Query: 301 EVVELTGPELVTTATVGSQRITACLPPRTAVGMGSAHAFTFDGTALHLFDPESG 354
            +VEL G E +    VG+  I     P T +  G          A  +F  ++G
Sbjct: 307 GMVELLGSERLIWGKVGNTSIVMRDDPDTTIRSGDQVRINLKPGAFSVFSAKTG 360


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: 324
Number of extensions: 10
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: 360
Length of database: 363
Length adjustment: 29
Effective length of query: 331
Effective length of database: 334
Effective search space:   110554
Effective search space used:   110554
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