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

GapMind for catabolism of small carbon sources

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

Align Ribose import ATP-binding protein RbsA 1; EC 7.5.2.7 (characterized, see rationale)
to candidate N515DRAFT_3232 N515DRAFT_3232 xylose ABC transporter ATP-binding protein

Query= uniprot:Q9WXX0
         (520 letters)



>lcl|FitnessBrowser__Dyella79:N515DRAFT_3232 N515DRAFT_3232 xylose
           ABC transporter ATP-binding protein
          Length = 513

 Score =  385 bits (989), Expect = e-111
 Identities = 220/504 (43%), Positives = 318/504 (63%), Gaps = 19/504 (3%)

Query: 14  ILKAKGIVKRFPGVVAVDNVDFEVYENEIVSLIGENGAGKSTLIKILTGVLKPDA--GEI 71
           + + +GI K F GV A+D +D  +   E + L GENGAGKSTL+K+L+GV    +  GEI
Sbjct: 7   LFEMRGIAKSFGGVKALDGIDLRLRAGECLGLCGENGAGKSTLMKVLSGVYPHGSWDGEI 66

Query: 72  LVNGERVEFHSPVDAFKKGISVIHQELNLCDNMTVAENIFLAYEAVRGQKRTLSSRVDEN 131
           L  G+ +   S  D+ + GI +IHQEL L   ++VAENIFL +E  R        R+D +
Sbjct: 67  LWQGQPLRARSVRDSERAGIVIIHQELMLVPQLSVAENIFLGHEITRP-----GGRMDYD 121

Query: 132 YMYTRSKELLDLIGAKFSPDAL-VRNLTTAQRQMVEICKALVKEPRIIFMDEPTSSLTVE 190
            MY ++  LL  +G      AL   +     +Q+ EI KAL K+ +++ +DEPTSSLT  
Sbjct: 122 AMYAKADALLQELGLHDVNVALPAMHYGGGHQQLFEIAKALAKQAKLLILDEPTSSLTSS 181

Query: 191 ETERLFEIIEMLKSRGISVVFVSHRLDEVMRISDRIVVMRDGKRIGELKKGEFDVDTIIK 250
           ETE L  I+E LK RG++ +++SH+LDEV R+ D + V+RDG+ I      E DVDT+I 
Sbjct: 182 ETEVLLGIVEDLKRRGVACIYISHKLDEVERVCDTVCVIRDGRHIATQPMHELDVDTLIT 241

Query: 251 MMVGREVEFFPHGIETRPGEIALEVRNLKWKD-------KVKNVSFEVRKGEVLGFAGLV 303
           +MVGR++E     IE   GE+  E R+    D       +V +VSF++R+GE+LG AGLV
Sbjct: 242 LMVGRKLENLYPRIEHAIGEVIFEARHATCLDPVNPQRKRVDDVSFQLRRGEILGIAGLV 301

Query: 304 GAGRTETMLLVFGV-NQKESGDIYVNGRKVEIKNPEDAIKMGIGLIPEDRKLQGLVLRMT 362
           GAGRTE +  +FG    K S ++++ GR ++I++P DAI+ G+G++PEDRK  G+V  + 
Sbjct: 302 GAGRTELVSAIFGAYTGKSSVELFLEGRPLKIRSPADAIRAGLGMVPEDRKRHGIVPLLG 361

Query: 363 VKDNIVLPSLKKISRWGLVLDERKEEEISEDYVKRLSIKTPSIYQITENLSGGNQQKVVL 422
           V DNI L +L   +  G + D ++E    E  +    +KT S       LSGGNQQK VL
Sbjct: 362 VGDNITLATLDHYAHAGHI-DRQRELVAIEAQIAERRVKTASPALPIARLSGGNQQKAVL 420

Query: 423 AKWLATNADILIFDEPTRGIDVGAKAEIHRMIRELAAQGKAVIMISSELPEILNLSDRIV 482
           AK L     +LI DEPTRG+DVGAKAEI+R+I ELAAQG A++++SSE+PE+L ++DR++
Sbjct: 421 AKMLLARPKVLILDEPTRGVDVGAKAEIYRLIFELAAQGVAIVLVSSEMPEVLGMADRVL 480

Query: 483 VMWEGEITAVLDNREKRVTQEEIM 506
           VM EG +     N  + +TQE+++
Sbjct: 481 VMGEGRLRGDFPN--QGLTQEQVL 502


Lambda     K      H
   0.319    0.138    0.381 

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: 660
Number of extensions: 36
Number of successful extensions: 9
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: 520
Length of database: 513
Length adjustment: 35
Effective length of query: 485
Effective length of database: 478
Effective search space:   231830
Effective search space used:   231830
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: 52 (24.6 bits)

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

Downloads

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

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:

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