Alignments for a candidate for Echvi_1871 in Sphingomonas koreensis DSMZ 15582

GapMind for catabolism of small carbon sources

Alignments for a candidate for Echvi_1871 in Sphingomonas koreensis DSMZ 15582

Align SSS sodium solute transporter (characterized, see rationale)
to candidate Ga0059261_1623 Ga0059261_1623 transporter, SSS family

Query= uniprot:L0FZF3
         (547 letters)



>FitnessBrowser__Korea:Ga0059261_1623
          Length = 549

 Score =  519 bits (1336), Expect = e-151
 Identities = 289/571 (50%), Positives = 368/571 (64%), Gaps = 57/571 (9%)

Query: 6   LDLVVFVAYCLLIITMGIVVSREKKGHVKDSKDYFLASKALPWWAVGASLIASNISAEQF 65
           +DL+V + Y + I  +   VSREK GH KD+ DYFLASK+LPWWA+GASLIA+NISAEQ 
Sbjct: 7   IDLIVVIVYAIGIFALAQWVSREKAGHAKDTSDYFLASKSLPWWAIGASLIAANISAEQI 66

Query: 66  IGMSGSGFALGLAISTYEWMAAATLLVVAIFFLPIYLKEGIYTMPQFLNRRYDGRVRTVM 125
           +GMSGSG+A+GLAI++YEWMAA TLL+V  +FLPI+LK  IYTMPQFL +R+   +RTVM
Sbjct: 67  VGMSGSGYAIGLAIASYEWMAALTLLIVGKWFLPIFLKNEIYTMPQFLEQRFGPTIRTVM 126

Query: 126 AIFWLLIYVFVNLTSVLYLGALSLETIMGVPLTYGIIGLALFAMVYSIYGGLKAVAWTDV 185
           A+FWL +Y+FVNLTS+L+LG++++  + GV     + GL  FA+VY + GGLKAVA TD+
Sbjct: 127 AVFWLALYIFVNLTSILWLGSIAVTQVAGVDQDIALFGLGAFALVYQLRGGLKAVALTDI 186

Query: 186 VQVVFLVAGGLATTYLALSLV-GDGDVWEGIGILRKAAPSHFSMIIEKGEMMIPDGSGGS 244
           VQV  LV GGL  +YL LS + GD  V  G   L    P  F MI      + PD     
Sbjct: 187 VQVTLLVLGGLVISYLTLSKIGGDAGVMGGFTRLTTELPGKFDMI------LAPD----- 235

Query: 245 RDAYLDLPGLSVLIGGMWIVNLNYWGCNQYITQRALAAKSLGEAQTGMVFAGFLKLLMPL 304
              Y DLPGLSVLIGGMWI NL+YWG NQYI QRALAAKSL EAQ G+VFA FLKLLMP+
Sbjct: 236 NPFYKDLPGLSVLIGGMWIANLSYWGFNQYIIQRALAAKSLSEAQKGVVFAAFLKLLMPV 295

Query: 305 IVVIPGIAAYVIVQKGADASFIESMTDPVTGLAKSDRAYPTLLHLLPPGLKGLAFAALTA 364
           I+V+PGIAA ++                   LAK D+AYPT++ LLP GL GL FAAL A
Sbjct: 296 IIVLPGIAAVIL----------------APDLAKPDQAYPTMMRLLPVGLLGLVFAALVA 339

Query: 365 AIVSSLASMANSTSTIFTIDIYKEFFNKN-------------------VSEGKQVTIGRI 405
           AI++S AS  NS +TIFT+D+Y +                          E + V +GR 
Sbjct: 340 AIIASTASKINSIATIFTLDLYAKAKGVQSRAQDAATASASGDSGLTAAHEKQLVRVGRT 399

Query: 406 TAVVAFIIAAIVA-PQLRQLDQAFQYIQEYTGFVSPGVFAIFIFGFFWKKTTSNAALTAA 464
           TAVVA ++A   A P L  LDQAFQYIQE++GFV+PG+  IF+ G FW + T   ALT A
Sbjct: 400 TAVVATLLAIFTARPLLGSLDQAFQYIQEFSGFVTPGITVIFLLGLFWPRATEAGALTGA 459

Query: 465 VLTIPLSAAF-------KVITPN-LPFIDRMGVVFLVLSVLIIAISLYEGKGKDSKKAIE 516
           V ++ LS  F        + T N +PF++RM +VF V   L + +SL      DS + I 
Sbjct: 460 VASVLLSFLFWFPADWGGIATLNAVPFMNRMMIVFFVSLALAVVVSLVRPAPADSNR-IT 518

Query: 517 VDAELFSTSTKFKVGAVLICGILVALYSVFW 547
           +    F T+T F V  V+I  IL+ALY+ +W
Sbjct: 519 MQGVSFGTTTSFNVAGVIIIMILIALYATWW 549


Lambda     K      H
   0.326    0.140    0.414 

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: 810
Number of extensions: 33
Number of successful extensions: 7
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: 547
Length of database: 549
Length adjustment: 36
Effective length of query: 511
Effective length of database: 513
Effective search space:   262143
Effective search space used:   262143
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 (21.6 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)
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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