GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Pseudomonas putida KT2440

Align ABC transporter for Glycerol, ATPase component 1 (characterized)
to candidate PP_2260 PP_2260 putative glycerol-phosphate ABC transporter, ATP-binding protein

Query= reanno::acidovorax_3H11:Ac3H11_791
         (363 letters)



>FitnessBrowser__Putida:PP_2260
          Length = 364

 Score =  330 bits (847), Expect = 3e-95
 Identities = 187/362 (51%), Positives = 238/362 (65%), Gaps = 15/362 (4%)

Query: 1   MQLALDSISKKVGAQTWLYDMSLALQSGAVTVLLGATQAGKTSLMRIMAGLDAPTAGRVT 60
           M L L+ +S+ V  Q W+ D SL  + G+  VLLG T AGKTSLMR+MAGLD P  GRV 
Sbjct: 1   MSLVLEQVSRSVDNQPWIVDASLRFEPGSFNVLLGRTLAGKTSLMRLMAGLDRPDRGRVL 60

Query: 61  VDGKDVTGMPVRDRNVAMVYQQFINYPSMKVAANIASPLKLR--GEKNIDARVREIASRL 118
           +DG+DVTG+PVR RNV+MVYQQFINYP++ V  NIASPL+     E  I  RV+E A  L
Sbjct: 61  MDGQDVTGVPVRQRNVSMVYQQFINYPTLSVYENIASPLRQARMAEDQIRRRVQETAEML 120

Query: 119 HIDMFLDRYPAELSGGQQQRVALARALAKGAPLMLLDEPLVNLDYKLREELREELTQLFA 178
            I+ +L R P ELSGGQQQR A+ARAL K A L+L DEPLVNLDYKLRE LR+EL +LFA
Sbjct: 121 RIETYLQRLPLELSGGQQQRTAMARALVKDASLILFDEPLVNLDYKLREGLRQELRELFA 180

Query: 179 AGQSTVVYATTEPGEALLLGGYTAVLDEGQLLQYGPTAEVFHAPNSLRVARAFSDPPMNL 238
           A     VYATTEP EAL LGG T ++ EG+++Q GPTAEV+  P+S+  A  FS+PP+NL
Sbjct: 181 ARHCIAVYATTEPNEALALGGTTTLVHEGRIVQSGPTAEVYQRPSSVLAAELFSEPPINL 240

Query: 239 MAASAT------AQGVRLQGGAELTLPLPQGAATAAGLTVGVRASALR-VHARPGDVSVA 291
           ++   T      AQ V     A+L  PL +G         GVR S +  V A   D+ +A
Sbjct: 241 VSGRITGNEVSLAQTVHFARNADLE-PLAEG-----DYRFGVRPSHIALVPAHDDDLELA 294

Query: 292 GVVELAEISGSDTFVHASTPWGDLVAQLTGVHYFELGTAITLHLDPAQAYVFGADGRLAQ 351
            +VELAEISGS+TF+H    +  +V  L GVH +++ T I + +   + +VF + G L Q
Sbjct: 295 VLVELAEISGSETFLHVRNEYWRMVLHLPGVHEYQVDTPIRVFIPTHKLFVFDSAGLLVQ 354

Query: 352 AP 353
           AP
Sbjct: 355 AP 356


Lambda     K      H
   0.318    0.133    0.375 

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: 347
Number of extensions: 17
Number of successful extensions: 3
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: 363
Length of database: 364
Length adjustment: 29
Effective length of query: 334
Effective length of database: 335
Effective search space:   111890
Effective search space used:   111890
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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 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