GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Desulfacinum infernum DSM 9756

Align ABC transporter for Glycerol, ATPase component 1 (characterized)
to candidate WP_073037049.1 BUB04_RS03680 ABC transporter ATP-binding protein

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



>NCBI__GCF_900129305.1:WP_073037049.1
          Length = 367

 Score =  356 bits (913), Expect = e-103
 Identities = 196/361 (54%), Positives = 249/361 (68%), Gaps = 13/361 (3%)

Query: 1   MQLALDSISKKVGAQTWLYDMSLALQSGAVTVLLGATQAGKTSLMRIMAGLDAPTAGRVT 60
           M L L+ + + V  +T L D++L   SG+  +LLG T AGKT+L+RIMAGLD PT GRV 
Sbjct: 1   MGLTLEHVDRIVDGETHLSDINLEFPSGSRNILLGRTLAGKTTLLRIMAGLDRPTRGRVL 60

Query: 61  VDGKDVTGMPVRDRNVAMVYQQFINYPSMKVAANIASPLKLRG--EKNIDARVREIASRL 118
           VDGKDVTG+ VR RNVAMVYQQFINYPS  V  NIASPL+L+G   + ID RVR++A  L
Sbjct: 61  VDGKDVTGVSVRKRNVAMVYQQFINYPSFTVYDNIASPLRLQGVPRREIDRRVRDVAEML 120

Query: 119 HIDMFLDRYPAELSGGQQQRVALARALAKGAPLMLLDEPLVNLDYKLREELREELTQLFA 178
            +  FLDR P++LSGGQQQR A+ARAL K A L+LLDEPLVNLDYKLREELREELT +F 
Sbjct: 121 RLTPFLDRLPSQLSGGQQQRTAIARALVKEADLLLLDEPLVNLDYKLREELREELTAIFE 180

Query: 179 AGQSTVVYATTEPGEALLLGGYTAVLDEGQLLQYGPTAEVFHAPNSLRVARAFSDPPMNL 238
            G+S VVY TTEP EAL+LGG   +LDEG++LQ GPT  V+H P S+R A  +SDPP+N 
Sbjct: 181 RGRSIVVYTTTEPTEALMLGGNVVILDEGRVLQSGPTDRVYHRPESMRAAEVYSDPPINY 240

Query: 239 MAASATAQGVRLQGGAELTLPLPQGAATAAGLT-----VGVRASALRVHARPG-DVSVAG 292
           +   A  +G + + G  +T PL    A   GL      +G+RA+   +  R   DV++  
Sbjct: 241 L--DAVVEGGQARIGERITFPL---VAHLEGLAPGRYHLGLRANRFFLKKRTDRDVALES 295

Query: 293 VVELAEISGSDTFVHASTPWGDLVAQLTGVHYFELGTAITLHLDPAQAYVFGADGRLAQA 352
           VVEL+EI+GS+TFVH S     LV   TG+   ++G A+T++ DPAQ +VF  +G L  A
Sbjct: 296 VVELSEINGSETFVHVSHQGFSLVVHETGIRSHKMGAAVTVYADPAQFFVFDQEGTLVAA 355

Query: 353 P 353
           P
Sbjct: 356 P 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: 367
Number of extensions: 16
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: 367
Length adjustment: 30
Effective length of query: 333
Effective length of database: 337
Effective search space:   112221
Effective search space used:   112221
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 Apr 09 2024. 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