GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Halomonas desiderata SP1

Align Spermidine/putrescine import ATP-binding protein PotA, component of The spermidine/putrescine uptake porter, PotABCD (characterized)
to candidate WP_086510882.1 BZY95_RS15925 ABC transporter ATP-binding protein

Query= TCDB::Q97Q42
         (385 letters)



>NCBI__GCF_002151265.1:WP_086510882.1
          Length = 354

 Score =  266 bits (681), Expect = 5e-76
 Identities = 146/334 (43%), Positives = 211/334 (63%), Gaps = 9/334 (2%)

Query: 20  TKVLKDINFELEEGKFYTLLGASGSGKSTILNIIAGLLDATTGDIMLDGVRINDIPTNKR 79
           T   +DI+ E+E+G+F +LLG SG GK+T L +IAG ++ T G I++DG  I     N+R
Sbjct: 16  TTAAEDISLEIEKGEFVSLLGPSGCGKTTTLQMIAGFVEPTRGRILMDGEDITHRKPNER 75

Query: 80  DVHTVFQSYALFPHMNVFENVAFPLRLRKIDKKEIEQRVAEVLKMVQLEGYEKRSIRKLS 139
            +  VFQSYALFPHM V ENV F L +R++   E  QRV EVL++V L+  + R  R+LS
Sbjct: 76  GIGIVFQSYALFPHMTVVENVRFGLEMRRVPATESRQRVGEVLELVHLDQLKDRYPRELS 135

Query: 140 GGQRQRVAIARAIINQPRVVLLDEPLSALDLKLRTDMQYELRELQQRLGITFVFVTHDQE 199
           GGQRQRVA+ARA++ QP ++LLDEPLS LD KLR DMQ ELR++QQ++G T + VTHDQ 
Sbjct: 136 GGQRQRVALARALVIQPPLLLLDEPLSNLDAKLREDMQIELRKIQQQVGTTTLMVTHDQS 195

Query: 200 EALAMSDWIFVMNDGEIVQSGTPVDIYDEPINHFVATFIGESNILPGTM----IEDYLVE 255
           EAL++SD + VMN G +VQ   P + Y+ P + FV++F+G++N+L G +     +   + 
Sbjct: 196 EALSLSDRVVVMNQGRVVQVDEPFNAYERPSDAFVSSFVGKTNLLTGLIGKKQGDQTSIR 255

Query: 256 FNGKRFEAVDGGMKPNEPVEVVIRPEDLRITLPEEGKLQVKVDTQLFRGVHYEIIAYDEL 315
                 E    G + +  V++ IRPE L +T    GKL+ +V T+LF G H+ +   D  
Sbjct: 256 LGDATLELTLNGPRTSNQVQISIRPEKLELTDCASGKLKGRVKTRLFLGNHW-LYQVDSS 314

Query: 316 GNEWMIH----STRKAIVGEEIGLDFEPEDIHIM 345
             E  I       R   VG+++G+ + P  I ++
Sbjct: 315 AGELFITQPNLGKRGVAVGDDVGVSWSPGAIRLL 348


Lambda     K      H
   0.318    0.138    0.386 

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: 293
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: 385
Length of database: 354
Length adjustment: 30
Effective length of query: 355
Effective length of database: 324
Effective search space:   115020
Effective search space used:   115020
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