Aligments for a candidate for xylG in Phaeobacter inhibens BS107

GapMind for catabolism of small carbon sources

Aligments for a candidate for xylG in Phaeobacter inhibens BS107

Align Xylose import ATP-binding protein XylG, component of Xylose transporter, XylFGH (XylF (R), 359 aas; XylG (C), 525 aas; XylH (M), 389 aas (characterized)
to candidate GFF2770 PGA1_c28130 ABC transporter, ATP-binding protein

Query= TCDB::A6LW11
         (525 letters)



>FitnessBrowser__Phaeo:GFF2770
          Length = 505

 Score =  256 bits (654), Expect = 1e-72
 Identities = 165/514 (32%), Positives = 272/514 (52%), Gaps = 14/514 (2%)

Query: 1   MSEYILEMRDIVKEFFGVKALDGVTLKVKKGEIHALCGENGAGKSTLMKVLSGEHPAGSY 60
           M++ +L ++ + K + GV A D V+  +  GE+HAL GENGAGKSTL+K++ G     S 
Sbjct: 1   MTQPLLSLQGLTKAYPGVVANDTVSFDIGAGEVHALLGENGAGKSTLVKMIYGLVKPDS- 59

Query: 61  SGKIIFEGKELSQTSIKDSESVGIAIIHQELALIKQLSIAENIFLGNEIGARGLVNFSEQ 120
            GK++  G+  +    + + + GIA++ Q  +L   L++AENI LG E     L + + Q
Sbjct: 60  -GKMLLHGEPYTPGEPRQARADGIAMVFQHFSLFDALNVAENIALGMETPP-ALRDLATQ 117

Query: 121 LNKTNELLNRVKLNVNPLTRAGDLGIGHQQLVEIAKALSKNAKLLILDEPSASLSEGEVE 180
           + K +E      L ++P    GDL  G +Q VEI + L ++ KLLI+DEP++ L+  EVE
Sbjct: 118 IRKVSETYG---LPLDPYRTVGDLSAGERQRVEIIRCLLQDPKLLIMDEPTSVLTPQEVE 174

Query: 181 VLMGILDDLRRDGVTCIYISHKLNEVTRICDNVTVIRDGSTIGQVPISEIDQDKLVQMMV 240
           +L   L  LR +G + +YISHKL E+  +CD+ T++R G  +G+   SE     + +MMV
Sbjct: 175 ILFQTLQKLRSEGTSILYISHKLEEIRTLCDHATILRLGKNVGECVPSETSARDMAEMMV 234

Query: 241 GREMKNLFPREEHKIGEEFFEIKNFNVLDPFNKNIKRVKNASFTLRRGEILGISGLVGSG 300
           G  ++    R    +G+   +I   +V  P +     +KN   T+R+GEILG+ G+ G+G
Sbjct: 235 GTALQTP-ERSGRALGDVALDISGLSVPAP-SAFGTALKNVHMTVRKGEILGVGGVAGNG 292

Query: 301 RTEMVASIYGSFQGQKSGEVYFEGKKIDIKNPNDALSKGIAMVPEDRKKDGIIAGMSVAK 360
           + E++  + G      +  V  +G  I    P      GI   PE+R        MS+ +
Sbjct: 293 QDELLGVLSGE-TTTAADAVTLDGAPIGNLGPVARRRLGILAAPEERLGHAAAPDMSLTE 351

Query: 361 NMTMSNLVK---YKRPLNVIDKDKEMMDVLKFIDEIKIKTASTELAIKNLSGGNQQKVIL 417
           N  ++   +     R        +E  +  K I    ++T   E A ++LSGGN QK ++
Sbjct: 352 NAMLTAATREGLASRGFLKWGLAQEFAE--KVIKSFDVRTPGPENAARSLSGGNLQKFVI 409

Query: 418 AKNLLAEPKILILDEPTRGIDVGAKYEIYKLIFKLAKQGISIIMVSSELPEVLGISDRVL 477
            + +L  P +L++++PT G+D  A   I + +  LA  G ++I +S +L E++ I+D   
Sbjct: 410 GREVLQRPDVLVVNQPTWGVDAAAAAAIRQSLLDLAAGGTAVICISQDLDELMEIADSFA 469

Query: 478 VMNEGEIKASLENNGLTQEMIMNYSVGKKNEEVS 511
            +NEG + A     GL+ + I     G    EV+
Sbjct: 470 ALNEGRLSAPRPTAGLSVDEIGLMMGGAHGMEVA 503


Lambda     K      H
   0.315    0.135    0.362 

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: 606
Number of extensions: 34
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: 525
Length of database: 505
Length adjustment: 35
Effective length of query: 490
Effective length of database: 470
Effective search space:   230300
Effective search space used:   230300
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 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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Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
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, 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