GapMind for catabolism of small carbon sources

 

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

Align D-mannose and D-mannitol transporter (characterized)
to candidate H281DRAFT_01516 H281DRAFT_01516 D-galactonate transporter

Query= reanno::pseudo5_N2C3_1:AO356_28540
         (430 letters)



>FitnessBrowser__Burk376:H281DRAFT_01516
          Length = 430

 Score =  459 bits (1181), Expect = e-134
 Identities = 227/417 (54%), Positives = 296/417 (70%), Gaps = 11/417 (2%)

Query: 1   MFGQGRSLIIIMLFLAGVINYLDRSALSVAAPFIQKDYGLSTGEMGMIFSSFFVGYAAFN 60
           M    R  ++ +LFLAGVINYLDRSALS+AAP IQKD   S  +MG++FSSFFVGYA FN
Sbjct: 1   MIKSQRWFVVALLFLAGVINYLDRSALSIAAPLIQKDLNFSHAQMGVVFSSFFVGYALFN 60

Query: 61  FIGGWAADRYGAKTTLLLAMVLWSLFSGLTVLTVGFASLVLIRILFGMGEGPLSVTTSKM 120
           F+GG  +D+ GAK     AM +WSLF G T L  G  SL+++R+LFGMGEGP S + SKM
Sbjct: 61  FVGGVLSDKVGAKRVFGTAMGVWSLFCGATALATGIGSLIVLRVLFGMGEGPFSSSNSKM 120

Query: 121 VNNWYTPKRRARAIGASMSGTPLGGAISGPVVGFIAVTYGWKISFIIIMLIGLVWAAVWF 180
           VNNW+  K  A AIG   SGTPLGGA++GPVVGF+AV +GW+ +F+ IML+GL+W   W 
Sbjct: 121 VNNWFPRKEVASAIGVISSGTPLGGALAGPVVGFMAVQFGWRWAFVAIMLLGLLWLVFWA 180

Query: 181 KFVKERPE------GEGAEDILRAEGQGELAAQPV----FPLRFYLKQPTVLFTSLAFFS 230
               E P+       +  + IL  +      A         L  +L++P +L T+ AFFS
Sbjct: 181 ATTTEHPQQNSRVTSDEMQLILAGQADEHALAHSADGSKLGLGHFLRKPIILATAFAFFS 240

Query: 231 YNYTLFFFLTWFPSYLTMAHGLNVKDMSIATVIPWVLGFLGLALGGFISDFVFKKTGRMM 290
           YNY LFFFL+WFP+YLT AH L++ DMSIATVIPWVLG +GLA GGFISD + + TG+ +
Sbjct: 241 YNYVLFFFLSWFPTYLTEAHHLSLHDMSIATVIPWVLGSIGLAAGGFISDLILRLTGKPL 300

Query: 291 FSRKVVLVTCLLACAVCIACAGMVTTLYPAVILVALAVFFLYLTGAIYWAIIQDTVPAAR 350
            SRK+VL TCL A AVC+A AG V +   AV L+++++FFLY+TGA+YWA+IQDTVP   
Sbjct: 301 LSRKIVLGTCLGAAAVCVALAGRVASTESAVALMSVSIFFLYVTGAVYWAVIQDTVPREH 360

Query: 351 VGGVSGFMHFLANTSGIVGPTLTGFLVQFT-GSFTSAFLLAGLLTVIGAVCVARYVK 406
           VGGV GF+H LAN +G++GP +TGF+VQ T G++ SAF+LAG + V+GAVC   +++
Sbjct: 361 VGGVGGFVHLLANLAGVIGPAVTGFIVQATHGAYGSAFVLAGGIAVLGAVCSLVWIR 417


Lambda     K      H
   0.329    0.142    0.439 

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: 632
Number of extensions: 24
Number of successful extensions: 3
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: 430
Length of database: 430
Length adjustment: 32
Effective length of query: 398
Effective length of database: 398
Effective search space:   158404
Effective search space used:   158404
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 51 (24.3 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:

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:

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:

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:

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