Alignments for a candidate for H281DRAFT_01113 in Paraburkholderia bryophila 376MFSha3.1

GapMind for catabolism of small carbon sources

Alignments for a candidate for H281DRAFT_01113 in Paraburkholderia bryophila 376MFSha3.1

Align deoxynucleoside transporter, ATPase component (characterized)
to candidate H281DRAFT_03380 H281DRAFT_03380 monosaccharide ABC transporter ATP-binding protein, CUT2 family

Query= reanno::Burk376:H281DRAFT_01113
         (515 letters)



>FitnessBrowser__Burk376:H281DRAFT_03380
          Length = 515

 Score =  357 bits (916), Expect = e-103
 Identities = 202/501 (40%), Positives = 303/501 (60%), Gaps = 12/501 (2%)

Query: 10  PLSQPFLEVVGVHKRFTGVHALRGVSLSFQRGQIYHLLGENGCGKSTLIKIISGAQPPDE 69
           P  +  L++ GV KRF GV AL G+ L  + G+++ + GENG GKSTL+KIISG    D+
Sbjct: 17  PAPREILQLKGVSKRFPGVVALDGIDLDLRSGEVHAVCGENGAGKSTLMKIISGQYHADD 76

Query: 70  GQLVIEGVPHARLSALEALAAGIETVYQDLSLLPNMSVAENVALTSELATHEGRLARTFD 129
           G +  EG P    S  +A AAGI  ++Q+L+L+P++SVAEN+ L       E +     D
Sbjct: 77  GVICYEGKPVQFASTSDAQAAGIAIIHQELNLVPHLSVAENIYLA-----REPKRGPFVD 131

Query: 130 RRVLAATAARALEAVGLPGNSEFQSTLIEQLPLATRQLVAIARAIASEAKFVIMDEPTTS 189
            R L A A R L+ +GL   +   +TL+  L +A +Q+V IA+A++ +A+ +IMDEPT+S
Sbjct: 132 YRTLNANAQRCLQRIGL---NVSPTTLVGALSIAQQQMVEIAKALSLDARVLIMDEPTSS 188

Query: 190 LTQKEVDNLIAVLANLRAQGVTVLFVSHKLDECYAIGGEVIVLRDGQKMAQGPIAEFTKA 249
           LT+ E   L  ++  LRA GV +L++SH+LDE   I   V VLRDG+ +A    A  T  
Sbjct: 189 LTESETVQLFRIIRELRADGVAILYISHRLDEMAEIVDRVTVLRDGRHIATSDFASTTIN 248

Query: 250 QISELMTGRHLSNERY--RESAHAQDIVLDVRGFTRAGQFSDVSFKLHGGEILGVTGLLD 307
           +I   M GR L ++ Y  RES   + +++ VR   R   F  +SF L  GEILG  GL+ 
Sbjct: 249 EIVARMVGRAL-DDAYPPRESVPTEQVLMRVRDLQRTDTFGPLSFDLRKGEILGFAGLMG 307

Query: 308 SGRNELARALAGVAPAQSGDVLLDGQQIALRTPSDAKRHRIGYVPEDRLNEGLFLDKPIR 367
           +GR E+ARA+ G     SG + L    + +R+P +A RH I Y+ EDR  +GL L  P+ 
Sbjct: 308 AGRTEVARAIFGAERLDSGSIQLGDTPVTIRSPREAIRHGIAYLSEDRKKDGLALSMPVA 367

Query: 368 DNVITAMISSLRDRFGQIDRTRAQALAEQTVKELQIATPGVDKPVQSLSGGNQQRVLIGR 427
            N+  + + ++  R G +  +   A+AE+ V+EL I TP V +  ++LSGGNQQ+++I +
Sbjct: 368 ANITLSNVRAISSR-GFLRFSEETAIAERYVRELAIRTPTVKQIARNLSGGNQQKIVISK 426

Query: 428 WLAIDPRVLILHGPTVGVDVGSKDIIYRIMQRLSQRGIGIILISDDLPELLQNCDRILMM 487
           WL    R+L    PT G+DVG+K  IY++M RL+  G+G++LIS +LPELL   DRI + 
Sbjct: 427 WLYRGSRILFFDEPTRGIDVGAKYAIYKLMDRLAADGVGVVLISSELPELLGMTDRIAVF 486

Query: 488 KKGHVSAEYRADELSEADLYH 508
            +G ++A     + S+ ++ H
Sbjct: 487 HEGLITAVLETRQTSQEEILH 507



 Score = 60.1 bits (144), Expect = 2e-13
 Identities = 52/228 (22%), Positives = 98/228 (42%), Gaps = 8/228 (3%)

Query: 34  VSLSFQRGQIYHLLGENGCGKSTLIKIISGAQPPDEGQLVIEGVPHARLSALEALAAGIE 93
           +S   ++G+I    G  G G++ + + I GA+  D G + +   P    S  EA+  GI 
Sbjct: 290 LSFDLRKGEILGFAGLMGAGRTEVARAIFGAERLDSGSIQLGDTPVTIRSPREAIRHGIA 349

Query: 94  TVYQDLS---LLPNMSVAENVALTSELATHEGRLARTFDRRVLAATAARALEAVGLPGNS 150
            + +D     L  +M VA N+ L++  A       R  +   +A    R L A+  P   
Sbjct: 350 YLSEDRKKDGLALSMPVAANITLSNVRAISSRGFLRFSEETAIAERYVREL-AIRTPTVK 408

Query: 151 EFQSTLIEQLPLATRQLVAIARAIASEAKFVIMDEPTTSLTQKEVDNLIAVLANLRAQGV 210
           +    +   L    +Q + I++ +   ++ +  DEPT  +       +  ++  L A GV
Sbjct: 409 Q----IARNLSGGNQQKIVISKWLYRGSRILFFDEPTRGIDVGAKYAIYKLMDRLAADGV 464

Query: 211 TVLFVSHKLDECYAIGGEVIVLRDGQKMAQGPIAEFTKAQISELMTGR 258
            V+ +S +L E   +   + V  +G   A     + ++ +I    +GR
Sbjct: 465 GVVLISSELPELLGMTDRIAVFHEGLITAVLETRQTSQEEILHYASGR 512


Lambda     K      H
   0.319    0.135    0.376 

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: 612
Number of extensions: 27
Number of successful extensions: 7
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: 515
Length of database: 515
Length adjustment: 35
Effective length of query: 480
Effective length of database: 480
Effective search space:   230400
Effective search space used:   230400
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.

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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