Alignments for a candidate for ytfR in Paraburkholderia bryophila 376MFSha3.1

GapMind for catabolism of small carbon sources

Alignments for a candidate for ytfR in Paraburkholderia bryophila 376MFSha3.1

Align galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) (characterized)
to candidate H281DRAFT_03380 H281DRAFT_03380 monosaccharide ABC transporter ATP-binding protein, CUT2 family

Query= ecocyc::YTFR-MONOMER
         (500 letters)



>FitnessBrowser__Burk376:H281DRAFT_03380
          Length = 515

 Score =  375 bits (963), Expect = e-108
 Identities = 201/493 (40%), Positives = 309/493 (62%), Gaps = 8/493 (1%)

Query: 7   QEILRTEGLSKFFPGVKALDNVDFSLRRGEIMALLGENGAGKSTLIKALTGVYHADRGTI 66
           +EIL+ +G+SK FPGV ALD +D  LR GE+ A+ GENGAGKSTL+K ++G YHAD G I
Sbjct: 20  REILQLKGVSKRFPGVVALDGIDLDLRSGEVHAVCGENGAGKSTLMKIISGQYHADDGVI 79

Query: 67  WLEGQAISPKNTAHAQQLGIGTVYQEVNLLPNMSVADNLFIGREPKRFGLLRRKEMEKRA 126
             EG+ +   +T+ AQ  GI  ++QE+NL+P++SVA+N+++ REPKR   +  + +   A
Sbjct: 80  CYEGKPVQFASTSDAQAAGIAIIHQELNLVPHLSVAENIYLAREPKRGPFVDYRTLNANA 139

Query: 127 TELMASYGFSLDVREPLNRFSVAMQQIVAICRAIDLSAKVLILDEPTASLDTQEVELLFD 186
              +   G ++     +   S+A QQ+V I +A+ L A+VLI+DEPT+SL   E   LF 
Sbjct: 140 QRCLQRIGLNVSPTTLVGALSIAQQQMVEIAKALSLDARVLIMDEPTSSLTESETVQLFR 199

Query: 187 LMRQLRDRGVSLIFVTHFLDQVYQVSDRITVLRNGSFVGCRETCELPQIELVKMMLGREL 246
           ++R+LR  GV++++++H LD++ ++ DR+TVLR+G  +   +       E+V  M+GR L
Sbjct: 200 IIRELRADGVAILYISHRLDEMAEIVDRVTVLRDGRHIATSDFASTTINEIVARMVGRAL 259

Query: 247 DTHALQRAGRTLLSDKPVAAFKNYGKKGTIAPFDLEVRPGEIVGLAGLLGSGRTETAEVI 306
           D     R   ++ +++ +   ++  +  T  P   ++R GEI+G AGL+G+GRTE A  I
Sbjct: 260 DDAYPPR--ESVPTEQVLMRVRDLQRTDTFGPLSFDLRKGEILGFAGLMGAGRTEVARAI 317

Query: 307 FGIKPADSGTALIKGKPQNLRSPHQASVLGIGFCPEDRKTDGIIAAASVRENIILA---L 363
           FG +  DSG+  +   P  +RSP +A   GI +  EDRK DG+  +  V  NI L+    
Sbjct: 318 FGAERLDSGSIQLGDTPVTIRSPREAIRHGIAYLSEDRKKDGLALSMPVAANITLSNVRA 377

Query: 364 QAQRGWLRPISRKEQQEIAERFIRQLGIRTPSTEQPIEFLSGGNQQKVLLSRWLLTRPQF 423
            + RG+LR     E+  IAER++R+L IRTP+ +Q    LSGGNQQK+++S+WL    + 
Sbjct: 378 ISSRGFLR---FSEETAIAERYVRELAIRTPTVKQIARNLSGGNQQKIVISKWLYRGSRI 434

Query: 424 LILDEPTRGIDVGAHAEIIRLIETLCADGLALLVISSELEELVGYADRVIIMRDRKQVAE 483
           L  DEPTRGIDVGA   I +L++ L ADG+ +++ISSEL EL+G  DR+ +  +    A 
Sbjct: 435 LFFDEPTRGIDVGAKYAIYKLMDRLAADGVGVVLISSELPELLGMTDRIAVFHEGLITAV 494

Query: 484 IPLAELSVPAIMN 496
           +   + S   I++
Sbjct: 495 LETRQTSQEEILH 507



 Score = 77.8 bits (190), Expect = 9e-19
 Identities = 61/227 (26%), Positives = 104/227 (45%), Gaps = 14/227 (6%)

Query: 28  VDFSLRRGEIMALLGENGAGKSTLIKALTGVYHADRGTIWLEGQAISPKNTAHAQQLGIG 87
           + F LR+GEI+   G  GAG++ + +A+ G    D G+I L    ++ ++   A + GI 
Sbjct: 290 LSFDLRKGEILGFAGLMGAGRTEVARAIFGAERLDSGSIQLGDTPVTIRSPREAIRHGIA 349

Query: 88  TVYQEVN---LLPNMSVADNLFIG--REPKRFGLLRRKEMEKRATELMASYGFSLDVREP 142
            + ++     L  +M VA N+ +   R     G LR  E     T +   Y   L +R P
Sbjct: 350 YLSEDRKKDGLALSMPVAANITLSNVRAISSRGFLRFSE----ETAIAERYVRELAIRTP 405

Query: 143 L-----NRFSVAMQQIVAICRAIDLSAKVLILDEPTASLDTQEVELLFDLMRQLRDRGVS 197
                    S   QQ + I + +   +++L  DEPT  +D      ++ LM +L   GV 
Sbjct: 406 TVKQIARNLSGGNQQKIVISKWLYRGSRILFFDEPTRGIDVGAKYAIYKLMDRLAADGVG 465

Query: 198 LIFVTHFLDQVYQVSDRITVLRNGSFVGCRETCELPQIELVKMMLGR 244
           ++ ++  L ++  ++DRI V   G      ET +  Q E++    GR
Sbjct: 466 VVLISSELPELLGMTDRIAVFHEGLITAVLETRQTSQEEILHYASGR 512


Lambda     K      H
   0.321    0.138    0.391 

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: 615
Number of extensions: 24
Number of successful extensions: 8
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 500
Length of database: 515
Length adjustment: 34
Effective length of query: 466
Effective length of database: 481
Effective search space:   224146
Effective search space used:   224146
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: 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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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
the source code
instructions for running GapMind on your computer

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