GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS17020 in Marinobacter adhaerens HP15

Align ABC-type sugar transport system, ATPase component protein (characterized, see rationale)
to candidate GFF4127 HP15_4067 spermidine/putrescine ABC transporter ATPase subunit

Query= uniprot:D8IPI1
         (406 letters)



>FitnessBrowser__Marino:GFF4127
          Length = 362

 Score =  219 bits (557), Expect = 1e-61
 Identities = 130/348 (37%), Positives = 193/348 (55%), Gaps = 9/348 (2%)

Query: 2   ADIHCQALAKHYAGGPPVLHPLDLHIGDGEFVVLLGPSGCGKSTMLRMIAGLEDISGGTL 61
           +D+ C+ L + +     V H + L +  G F  +LGPSGCGK+T+LR++AG +    G +
Sbjct: 3   SDLFCEGLVRRFGSNAAVDH-VSLDVPAGTFFSILGPSGCGKTTLLRLLAGFDKPDQGDI 61

Query: 62  RIGGTVVNDLPARERNVAMVFQNYALYPHMSVYDNIAFGLRRLKRPAAEIDRRVREVAAL 121
            I G  +ND+P   R V MVFQ+ AL+P M+V DNIA+GL+R K P  E  +R+  V   
Sbjct: 62  HIRGERMNDVPPNRRPVNMVFQHLALFPTMTVGDNIAYGLKRRKMPLVERRKRIARVLEQ 121

Query: 122 LNLEALLERKPRAMSGGQQQRAAIARAIIKTPSVFLFDEPLSNLDAKLRAQLRGDIKRLH 181
           + L  L  R P+ +SGGQ+QR A+AR ++  P++ L DEPL  LD KLR Q++ ++K L 
Sbjct: 122 VGLPDLEHRNPQELSGGQRQRVALARCLVLEPTLLLLDEPLGALDLKLREQMKVELKHLQ 181

Query: 182 QRLRTTTVYVTHDQLEAMTLADRVILMQDGRIVQAGSPAELYRYPRNLFAAGFIGTPAMN 241
           ++  TT VY+THDQ EAM ++D+V +M+DGR  Q   P ELYR P   F AGF+G    N
Sbjct: 182 KQFGTTFVYITHDQSEAMVMSDQVAVMRDGRFDQVAPPEELYREPATPFVAGFVGD--NN 239

Query: 242 FLSGTVQRQDGQLFIETAHQRWALTGERFS-RLRHAMAVKLAVRPDHVRIAGEREPAASL 300
            LSG +      L          + G   S  L+     +L +RP+ + ++G+       
Sbjct: 240 RLSGELVSVRDSLAELRLDDGVLVQGRVASDNLQAGHRAELYIRPESLVLSGDALSPGFS 299

Query: 301 TCPVSVELVEILGADALLTTRCGDQTLTALVPADRLPQPGATLTLALD 348
           +    V      GA++ +      Q + A     RLPQ G+   L++D
Sbjct: 300 SMQAKVRTTLFDGANSRVEAETCGQPVYA-----RLPQDGSAPRLSVD 342


Lambda     K      H
   0.321    0.137    0.403 

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: 379
Number of extensions: 16
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: 406
Length of database: 362
Length adjustment: 30
Effective length of query: 376
Effective length of database: 332
Effective search space:   124832
Effective search space used:   124832
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: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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