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

GapMind for catabolism of small carbon sources

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

Align Xylonate dehydratase (EC 4.2.1.82) (characterized)
to candidate H281DRAFT_06137 H281DRAFT_06137 dihydroxyacid dehydratase (EC 4.2.1.9)

Query= reanno::pseudo5_N2C3_1:AO356_28760
         (594 letters)



>FitnessBrowser__Burk376:H281DRAFT_06137
          Length = 583

 Score =  340 bits (873), Expect = 7e-98
 Identities = 196/529 (37%), Positives = 298/529 (56%), Gaps = 15/529 (2%)

Query: 45  RPIIGIAQTGSDLTPCNRHHLELAQRVKAGIRDAGGIPMEFPVHPIAEQSRRPTAALDRN 104
           RP+IGI  TGS    C+ +  +L + VK G+  AGG+P++FP   + E    PT+   RN
Sbjct: 50  RPVIGIVNTGSGFNACHGNMPQLVEAVKRGVMLAGGLPVDFPTISVHESFSSPTSMYLRN 109

Query: 105 LAYLGLVEILHGYPLDGVVLTTGCDKTTPACLMAAATTDLPAIVLSGGPMLDGHHKGELI 164
           L  +   E++   P+D VVL  GCDKT PA LM AA+ ++PAI L  G ML G H+ E +
Sbjct: 110 LMSMDTEEMIRAQPMDAVVLIGGCDKTVPAQLMGAASAEIPAIQLVTGSMLTGSHRSERV 169

Query: 165 GSGTVLWHARNLMAAGEIDYEGFMEMTTAASPSVGHCNTMGTALSMNALAEALGMSLPGC 224
           G+ T          A EID E   ++      SVG C+ MGTA +M  +AEALGM++PG 
Sbjct: 170 GACTDCRRYWGKFRASEIDQEEINDVNNQLVASVGTCSVMGTASTMACIAEALGMTVPGG 229

Query: 225 ASIPAPYRERGQMAYATGKRICELVLQDIRPSQIMTRQAFENAIAVASALGASSNCPPHL 284
           A+ PA   +R ++A  TG    +L  + +   +I+T +AFENA+ V  A+G S+N   HL
Sbjct: 230 ATPPAVTADRIRVAEQTGTTAVKLASERLTIDKILTPKAFENAMRVLLAIGGSTNAIVHL 289

Query: 285 IAIARHMGVELSLDDWQRIGEDVPLLVNCMPAGKYLGEGFHRAGGVPSVMHELQKAGRLH 344
            A+A  +G ++ LD   R+G++ P+L++  P G++  E FH+AGGV +++ EL+    LH
Sbjct: 290 SAVAGRLGHKIGLDSLDRMGKETPVLLDLKPTGQHYMEDFHKAGGVATLLRELKPL--LH 347

Query: 345 EDCATVSGRTIGE-IVSSSLTSNADVIHPFDTPLKHRAGFIVLSGNFF-DSAIMKMSVVG 402
            D  TVSG T+GE I +S    + DV+  F  P+  + G  V+ GN     AI+K S   
Sbjct: 348 LDAMTVSGHTLGEQIEASGPGFSQDVVRSFSQPIYPQGGLAVVRGNLAPGGAIIKQSAAD 407

Query: 403 EAFRKTYLSEPGAENSFEARAIVFEGPEDYHARIDDPALDIDERCILVIRGVGTVGYPGS 462
               +            E RA+VFE  ED   R+DD +LD+    +LV++ +G VG PG 
Sbjct: 408 PKLME-----------HEGRAVVFENLEDLINRVDDESLDVKADDVLVLKNIGPVGAPGM 456

Query: 463 AEVVNMAPPAALIKQGIDSLPCLGDGRQSGTSASPSILNMSPEAAVGGGLALLQTNDRLK 522
            E   +  P  L + G+  +  + DGR SGT+    +L+++PEAA GG  A +Q  DR++
Sbjct: 457 PEAGYIPIPRKLARAGVKDMVRISDGRMSGTAFGTIVLHVTPEAAAGGPFAYVQNGDRIR 516

Query: 523 VDLNTRTVNLLIDDEEMARRRLEWTPNIPPSQTPWQELYRQLVGQLSTG 571
           + ++ R V+LL+ DE++ +R  +     P +   +++L+ Q V Q   G
Sbjct: 517 LSVSNREVSLLVSDEKLKQRAADKPIKRPTADRGYRKLFLQTVTQADEG 565


Lambda     K      H
   0.319    0.135    0.407 

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: 895
Number of extensions: 55
Number of successful extensions: 4
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: 594
Length of database: 583
Length adjustment: 37
Effective length of query: 557
Effective length of database: 546
Effective search space:   304122
Effective search space used:   304122
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: 53 (25.0 bits)

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

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Protein sequences (fasta format)
Organisms (tab-delimited)
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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