Alignments for a candidate for PS417_11890 in Paraburkholderia bryophila 376MFSha3.1

GapMind for catabolism of small carbon sources

Alignments for a candidate for PS417_11890 in Paraburkholderia bryophila 376MFSha3.1

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

Query= reanno::pseudo3_N2E3:AO353_21385
         (521 letters)



>FitnessBrowser__Burk376:H281DRAFT_03380
          Length = 515

 Score =  442 bits (1138), Expect = e-128
 Identities = 237/493 (48%), Positives = 324/493 (65%), Gaps = 2/493 (0%)

Query: 27  LLEIINVSKGFPGVVALSDVQLRVRPGSVLALMGENGAGKSTLMKIIAGIYQPDAGELRL 86
           +L++  VSK FPGVVAL  + L +R G V A+ GENGAGKSTLMKII+G Y  D G +  
Sbjct: 22  ILQLKGVSKRFPGVVALDGIDLDLRSGEVHAVCGENGAGKSTLMKIISGQYHADDGVICY 81

Query: 87  RGKPVTFDTPLAALQAGIAMIHQELNLMPHMSIAENIWIGREQLNGFHMIDHREMHRCTA 146
            GKPV F +   A  AGIA+IHQELNL+PH+S+AENI++ RE   G   +D+R ++    
Sbjct: 82  EGKPVQFASTSDAQAAGIAIIHQELNLVPHLSVAENIYLAREPKRG-PFVDYRTLNANAQ 140

Query: 147 QLLERLRINLDPEEQVGNLSIAERQMVEIAKAVSYDSDILIMDEPTSAITDKEVAHLFSI 206
           + L+R+ +N+ P   VG LSIA++QMVEIAKA+S D+ +LIMDEPTS++T+ E   LF I
Sbjct: 141 RCLQRIGLNVSPTTLVGALSIAQQQMVEIAKALSLDARVLIMDEPTSSLTESETVQLFRI 200

Query: 207 IADLKAQGKGIIYITHKMNEVFSIADEVAVFRDGAYIGLQRADSMDGDSLISMMVGRELS 266
           I +L+A G  I+YI+H+++E+  I D V V RDG +I      S   + +++ MVGR L 
Sbjct: 201 IRELRADGVAILYISHRLDEMAEIVDRVTVLRDGRHIATSDFASTTINEIVARMVGRALD 260

Query: 267 QLFPVREK-PIGDLLMSVRDLRLDGVFKGVSFDLHAGEILGIAGLMGSGRTNVAEAIFGI 325
             +P RE  P   +LM VRDL+    F  +SFDL  GEILG AGLMG+GRT VA AIFG 
Sbjct: 261 DAYPPRESVPTEQVLMRVRDLQRTDTFGPLSFDLRKGEILGFAGLMGAGRTEVARAIFGA 320

Query: 326 TPSDGGEICLDGQPVRISDPHMAIEKGFALLTEDRKLSGLFPCLSVLENMEMAVLPHYAG 385
              D G I L   PV I  P  AI  G A L+EDRK  GL   + V  N+ ++ +   + 
Sbjct: 321 ERLDSGSIQLGDTPVTIRSPREAIRHGIAYLSEDRKKDGLALSMPVAANITLSNVRAISS 380

Query: 386 NGFIQQKALRALCEDMCKKLRVKTPSLEQCIDTLSGGNQQKALLARWLMTNPRILILDEP 445
            GF++     A+ E   ++L ++TP+++Q    LSGGNQQK ++++WL    RIL  DEP
Sbjct: 381 RGFLRFSEETAIAERYVRELAIRTPTVKQIARNLSGGNQQKIVISKWLYRGSRILFFDEP 440

Query: 446 TRGIDVGAKAEIYRLISYLASEGMAVIMISSELPEVLGMSDRVMVMHEGDLMGTLDRSEA 505
           TRGIDVGAK  IY+L+  LA++G+ V++ISSELPE+LGM+DR+ V HEG +   L+  + 
Sbjct: 441 TRGIDVGAKYAIYKLMDRLAADGVGVVLISSELPELLGMTDRIAVFHEGLITAVLETRQT 500

Query: 506 TQERVMQLASGMS 518
           +QE ++  ASG S
Sbjct: 501 SQEEILHYASGRS 513



 Score =  102 bits (253), Expect = 4e-26
 Identities = 69/243 (28%), Positives = 123/243 (50%), Gaps = 15/243 (6%)

Query: 286 LRLDGVFK---------GVSFDLHAGEILGIAGLMGSGRTNVAEAIFGITPSDGGEICLD 336
           L+L GV K         G+  DL +GE+  + G  G+G++ + + I G   +D G IC +
Sbjct: 23  LQLKGVSKRFPGVVALDGIDLDLRSGEVHAVCGENGAGKSTLMKIISGQYHADDGVICYE 82

Query: 337 GQPVRISDPHMAIEKGFALLTEDRKLSGLFPCLSVLENMEMAVLPHYAGNGFIQQKALRA 396
           G+PV+ +    A   G A++ ++  L    P LSV EN+ +A  P      F+  + L A
Sbjct: 83  GKPVQFASTSDAQAAGIAIIHQELNL---VPHLSVAENIYLAREPKRGP--FVDYRTLNA 137

Query: 397 LCEDMCKKLRVKTPSLEQCIDTLSGGNQQKALLARWLMTNPRILILDEPTRGIDVGAKAE 456
             +   +++ +   S    +  LS   QQ   +A+ L  + R+LI+DEPT  +      +
Sbjct: 138 NAQRCLQRIGLNV-SPTTLVGALSIAQQQMVEIAKALSLDARVLIMDEPTSSLTESETVQ 196

Query: 457 IYRLISYLASEGMAVIMISSELPEVLGMSDRVMVMHEGDLMGTLDRSEATQERVMQLASG 516
           ++R+I  L ++G+A++ IS  L E+  + DRV V+ +G  + T D +  T   ++    G
Sbjct: 197 LFRIIRELRADGVAILYISHRLDEMAEIVDRVTVLRDGRHIATSDFASTTINEIVARMVG 256

Query: 517 MSV 519
            ++
Sbjct: 257 RAL 259


Lambda     K      H
   0.321    0.137    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: 656
Number of extensions: 19
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: 521
Length of database: 515
Length adjustment: 35
Effective length of query: 486
Effective length of database: 480
Effective search space:   233280
Effective search space used:   233280
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, 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