GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Dinoroseobacter shibae DFL-12

Align Spermidine/putrescine import ATP-binding protein PotA, component of The spermidine/putrescine uptake porter, PotABCD (characterized)
to candidate 3608728 Dshi_2120 ABC transporter related (RefSeq)

Query= TCDB::Q97Q42
         (385 letters)



>FitnessBrowser__Dino:3608728
          Length = 376

 Score =  234 bits (596), Expect = 4e-66
 Identities = 138/361 (38%), Positives = 212/361 (58%), Gaps = 22/361 (6%)

Query: 3   KPIIEFKNVSKVFEDSNTKVLKDINFELEEGKFYTLLGASGSGKSTILNIIAGLLDATTG 62
           +PI++F NV K F   +   +K  +FE+  G+F  ++G+SG GK+T L ++AGL D T G
Sbjct: 12  EPIVKFDNVVKRF--GSFTAVKKADFEIGRGEFLAIMGSSGCGKTTTLRMLAGLEDPTEG 69

Query: 63  DIMLDGVRINDIPTNKRDVHTVFQSYALFPHMNVFENVAFPLRLRKIDKKEIEQRVAEVL 122
            I LDG ++N   T  RD   V+QS ALFP + V ENV F L++R I K+E  QR  + L
Sbjct: 70  AIYLDGEQVNGKATWDRDTPMVWQSLALFPFLTVQENVEFALKMRGIGKEERRQRADKWL 129

Query: 123 KMVQLEGYEKRSIRKLSGGQRQRVAIARAIINQPRVVLLDEPLSALDLKLRTDMQYELRE 182
             +Q+  +  R+I +LSGGQ+QRVA+ARA++ +P+++LLDEPLSALD  L+  MQ  L  
Sbjct: 130 DKMQITEFADRNINQLSGGQKQRVALARALVTEPKILLLDEPLSALDAHLKVRMQSVLSN 189

Query: 183 LQQRLGITFVFVTHDQEEALAMSDWIFVMNDGEIVQSGTPVDIYDEPINHFVATFIGESN 242
           LQ+ LGITFV+VTH   EA +M+D + +M+ G+I Q GTP +IY EP N FVA F+G +N
Sbjct: 190 LQKDLGITFVYVTHSMSEAFSMADRVVIMSRGQIEQIGTPEEIYREPHNRFVAEFLGSAN 249

Query: 243 ILPGTM---IED--YLVEFNG-----KRFEAVDGGMKPNEPVEVVIRPEDLRITLPEEGK 292
           I  G +    ED  + V + G      + E  +   +  + V  ++  E+++++LP+ G+
Sbjct: 250 IFDGVVEGPAEDGGWRVSYEGGETVLDKSELAEA--RKGQAVTFIVSAENMQLSLPDSGQ 307

Query: 293 --LQVKVDTQLFRGVHYEIIAYDELGNEWMIHSTRKAI------VGEEIGLDFEPEDIHI 344
             +   V  + F G    +      G E  +  T + +       G  I + + P+  H+
Sbjct: 308 PGIAASVAGEEFIGGTAMVFLETATGQELKVQKTHEELSQLDLHAGSRIIVHWAPDSCHV 367

Query: 345 M 345
           +
Sbjct: 368 L 368


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: 330
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: 385
Length of database: 376
Length adjustment: 30
Effective length of query: 355
Effective length of database: 346
Effective search space:   122830
Effective search space used:   122830
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: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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