GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Pseudomonas benzenivorans DSM 8628

Align ABC transporter for Glycerol, ATPase component 1 (characterized)
to candidate WP_090438526.1 BLS63_RS00940 ABC transporter ATP-binding protein

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



>NCBI__GCF_900100495.1:WP_090438526.1
          Length = 364

 Score =  328 bits (842), Expect = 1e-94
 Identities = 177/358 (49%), Positives = 236/358 (65%), Gaps = 3/358 (0%)

Query: 1   MQLALDSISKKVGAQTWLYDMSLALQSGAVTVLLGATQAGKTSLMRIMAGLDAPTAGRVT 60
           M L L+ +S+ V  Q ++ D  L  + G+  VLLG T AGKTSLMR++AGLD PT+GR+ 
Sbjct: 1   MSLTLEHVSRIVDNQVYIDDACLNFEPGSFNVLLGRTLAGKTSLMRLLAGLDRPTSGRIL 60

Query: 61  VDGKDVTGMPVRDRNVAMVYQQFINYPSMKVAANIASPLKLRG--EKNIDARVREIASRL 118
           ++G DVTG+PVR RNV+MVYQQFINYP+M V  NIASPL+  G  +  I+ +V+E A  L
Sbjct: 61  MNGADVTGVPVRKRNVSMVYQQFINYPTMTVFENIASPLRQAGVAQAEIERKVQETARML 120

Query: 119 HIDMFLDRYPAELSGGQQQRVALARALAKGAPLMLLDEPLVNLDYKLREELREELTQLFA 178
           HI+  L R+P ELSGGQQQR A+ARAL K A L+L DEPLVNLDYKLREELR+E+ +LF 
Sbjct: 121 HIENLLRRHPLELSGGQQQRTAMARALVKDADLVLFDEPLVNLDYKLREELRQEMRELFQ 180

Query: 179 AGQSTVVYATTEPGEALLLGGYTAVLDEGQLLQYGPTAEVFHAPNSLRVARAFSDPPMNL 238
           A ++  +YATTEP EAL LGG T +L EG+++Q G TAEV+H P  +  A  FS+PP+NL
Sbjct: 181 ARRTIAIYATTEPNEALALGGTTTILHEGRVVQSGKTAEVYHRPQQVLAAELFSEPPINL 240

Query: 239 MAASATAQGVRLQGGAELTLPLPQGAATAAGLTVGVRASAL-RVHARPGDVSVAGVVELA 297
           M+   +   V  +      L              GVR S +  V +   D+ +A  V+LA
Sbjct: 241 MSGGISGTEVSFEDAVHFPLNPDLRGLGEGAYRFGVRPSHIGLVPSNDDDLELAVTVDLA 300

Query: 298 EISGSDTFVHASTPWGDLVAQLTGVHYFELGTAITLHLDPAQAYVFGADGRLAQAPAR 355
           EISGS+TF+H       LV  L GVH +++ T I +++   + +VF   G+LAQAP+R
Sbjct: 301 EISGSETFLHVRNEHFTLVLHLPGVHEYDVDTPILVYIPTHKLFVFDTRGKLAQAPSR 358


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: 340
Number of extensions: 14
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 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