GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Cereibacter sphaeroides ATCC 17029

Align spermidine/putrescine ABC transporter, ATP-binding protein PotA; EC 3.6.3.31 (characterized)
to candidate WP_011842041.1 RSPH17029_RS15320 ABC transporter ATP-binding protein

Query= CharProtDB::CH_024626
         (378 letters)



>NCBI__GCF_000015985.1:WP_011842041.1
          Length = 372

 Score =  267 bits (682), Expect = 4e-76
 Identities = 153/323 (47%), Positives = 200/323 (61%), Gaps = 10/323 (3%)

Query: 20  LAGIRKCFDGKEVIPQLDLTINNGEFLTLLGPSGCGKTTVLRLIAGLETVDSGRIMLDNE 79
           L+ +   F   +VIP L L++  GE +  LGPSGCGKTT LR+IAGL     GRI +   
Sbjct: 24  LSEVGMTFGTLDVIPSLSLSVRRGEMVAFLGPSGCGKTTTLRMIAGLLDPTRGRISVGGR 83

Query: 80  DITHVPAENRYVNTVFQSYALFPHMTVFENVAFGLRMQKTPAAEITPRVMEALRMVQLET 139
           +ITH+P  +R +  VFQSYALFPHMTV +NVAFGL M++   AEI  RV  AL MVQL  
Sbjct: 84  EITHLPVHDRDMGMVFQSYALFPHMTVAQNVAFGLEMRRMAKAEIRSRVERALAMVQLGH 143

Query: 140 FAQRKPHQLSGGQQQRVAIARAVVNKPRLLLLDESLSALDYKLRKQMQNELKALQRKLGI 199
            A RKP  LSGGQQQRVA+ARA+V +P +LLLDE LS LD KLR +M+ ++++LQ++ GI
Sbjct: 144 LAGRKPKALSGGQQQRVALARALVVEPSILLLDEPLSNLDAKLRDEMRVQIRSLQQQSGI 203

Query: 200 TFVFVTHDQEEALTMSDRIVVMRDGRIEQDGTPREIYEEPKNLFVAGFIGEINMFNATVI 259
           T VFVTHDQ EAL+M DRIVVMR G +EQ GTP EIYE P   FVA F+G  N  +  V 
Sbjct: 204 TAVFVTHDQVEALSMCDRIVVMRGGHVEQFGTPNEIYERPATPFVASFVGRTNRLSGRV- 262

Query: 260 ERLDEQRVRANVEGRECNIYVNFAVEPGQKLHVLLRPEDLRVEEINDDNHA--EGLIGYV 317
               +   R  +EGR           P   + VL+RP  + +    +D  A    L G +
Sbjct: 263 ----DPSGRLLIEGRPVAAEGQL---PQGAVEVLVRPHRMSLRAAAEDQPAGLNSLPGVL 315

Query: 318 RERNYKGMTLESVVELENGKMVM 340
               + G  +++ V +  G++ +
Sbjct: 316 TGATFVGDLIQATVRIGGGEITV 338


Lambda     K      H
   0.319    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: 319
Number of extensions: 11
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: 378
Length of database: 372
Length adjustment: 30
Effective length of query: 348
Effective length of database: 342
Effective search space:   119016
Effective search space used:   119016
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 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 10 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