Aligments for a candidate for nupA in Dyella japonica UNC79MFTsu3.2

GapMind for catabolism of small carbon sources

Aligments for a candidate for nupA in Dyella japonica UNC79MFTsu3.2

Align Purine/cytidine ABC transporter ATP-binding protein, component of General nucleoside uptake porter, NupABC/BmpA (transports all common nucleosides as well as 5-fluorocytidine, inosine, deoxyuridine and xanthosine) (Martinussen et al., 2010) (Most similar to 3.A.1.2.12). NupA is 506aas with two ABC (C) domains. NupB has 8 predicted TMSs, NupC has 9 or 10 predicted TMSs in a 4 + 1 (or 2) + 4 arrangement (characterized)
to candidate N515DRAFT_2413 N515DRAFT_2413 simple sugar transport system ATP-binding protein

Query= TCDB::A2RKA7
         (506 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2413
          Length = 505

 Score =  255 bits (651), Expect = 3e-72
 Identities = 165/503 (32%), Positives = 267/503 (53%), Gaps = 14/503 (2%)

Query: 2   ANETVIQMIDVTKRFGDFVANDKVNLELKKGEIHALLGENGAGKSTLMNILSGLLEPSEG 61
           A   V+Q   + KRFG  +A D V+L L+ GE+HAL+G+NGAGKSTL+ +L+G+  P  G
Sbjct: 8   ARPVVLQARGLGKRFGATLALDGVDLALRAGEVHALMGQNGAGKSTLIKLLTGVERPDRG 67

Query: 62  EVHVKGKLENIDSPSKAANLGIGMVHQHFMLVDAFTVTENIILGNEVTKG--INLDLKTA 119
            V + G++    +P +A   GIG V+Q   L    +V EN+  G    +     +D +  
Sbjct: 68  SVELDGRVIAPSTPMEAQRDGIGTVYQEVNLCPNLSVAENLYAGRYPRRRRLRMIDWRQV 127

Query: 120 KKKILELSERYGLSVEPDALIRDISVGQQQRVEILKTLYRGADILIFDEPTAVLTPAEIT 179
           +     L  +  L ++ DA +    V  +Q V I + L   A +LI DEPT+ L   E+ 
Sbjct: 128 RDGARSLLRQLHLELDVDAPLGSYPVAIRQMVAIARALGVSARVLILDEPTSSLDEGEVR 187

Query: 180 ELMQIMKNLIKEGKSIILITHKLDEIRAVADRITVIRRGKSIDTVELGDKTNQELAELMV 239
           EL +++  L + G +I+ +TH LD++ AV+DRITV+R G  +    + D     L   MV
Sbjct: 188 ELFRVIAQLRERGMAILFVTHFLDQVYAVSDRITVLRDGCRVGEYAVADLPPAALVNAMV 247

Query: 240 GRSVSFI--TEKAAAQPKDVVLEIKDLNIKESRGSLKVKGLSLDVRAGEIVGVAGIDGNG 297
           GR +  +   +   A P D    I D      RG  K+  + L VR GE++G+ G+ G+G
Sbjct: 248 GRDLPTVAGADAERAPPPDAPPAI-DAQGLGCRG--KLHPVDLQVRRGEMLGLGGLLGSG 304

Query: 298 QTELVKAITGLTKVDSGSIKLHNKDITNQRPRKITEQSVGHVPEDRHRDGLVLEMTVAEN 357
           +TEL + + GL + + G +++  + +  + P     + +   PE+R  DG+V E++V EN
Sbjct: 305 RTELARLLFGLDRAERGELRIGGERVELKHPADAVVRGLALCPEERKTDGIVAELSVREN 364

Query: 358 IALQTYYKPPMSKYGFLDYNKINSH--ARELMEEFDVRGAGEWVSASSLSGGNQQKAIIA 415
           I L        ++ G+   ++      AR+L++   ++ A        LSGGNQQK ++A
Sbjct: 365 IVLAL-----QARQGWRGMSRARQDELARQLVQALGIKAADIETPVGLLSGGNQQKVMLA 419

Query: 416 REIDRNPDLLIVSQPTRGLDVGAIEYIHKRLIQARDEGKAVLVISFELDEILNVSDRIAV 475
           R +   P LLI+ +PTRG+DV A + +   + +    G AVL IS E  E+    DRIAV
Sbjct: 420 RWLVTEPRLLILDEPTRGIDVAAKQELMAEVTRRAHAGMAVLFISAETGELTRWCDRIAV 479

Query: 476 IHDGQIQGIVSPETTTKQELGIL 498
           + + +  G +   +T  + L ++
Sbjct: 480 MRERRKAGELPGGSTEARVLAMI 502


Lambda     K      H
   0.315    0.135    0.365 

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: 623
Number of extensions: 38
Number of successful extensions: 8
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: 506
Length of database: 505
Length adjustment: 34
Effective length of query: 472
Effective length of database: 471
Effective search space:   222312
Effective search space used:   222312
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: 42 (22.0 bits)
S2: 52 (24.6 bits)

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

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Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources