Alignments for a candidate for fruI in Kocuria flava HO-9041

GapMind for catabolism of small carbon sources

Alignments for a candidate for fruI in Kocuria flava HO-9041

Align The fructose inducible fructose/xylitol porter, FruI (characterized)
to candidate WP_058858172.1 AS188_RS06520 PTS transporter subunit EIIA

Query= TCDB::Q1LZ59
         (655 letters)



>NCBI__GCF_001482365.1:WP_058858172.1
          Length = 694

 Score =  363 bits (931), Expect = e-104
 Identities = 242/700 (34%), Positives = 365/700 (52%), Gaps = 78/700 (11%)

Query: 3   IQDLLNKDVMLLDLQATTKEAAIDEMVSKLVEQ-GIVTDFDTFKAGIMNREVQTSTGLGD 61
           + +L+  D++ LD      +A +   ++ LV++ G     D   A  + RE +T+TG+  
Sbjct: 1   MSELITPDLVQLDQDLGEDKATVIGQLAALVQRAGRAEQLDGLLADAIAREDKTATGIPG 60

Query: 62  GIAMPHSKNKAVKEATVLFAKSNKGVDYEALDGEPVDLFFMIAAPDGANDTHLAALAELS 121
           GIA+PH ++ AV   T+  A+ +  VD+ A DG P DL F IAAP+GA+ THL  LA+L+
Sbjct: 61  GIAIPHCRSTAVTAPTLAMARLDPKVDFGAKDG-PADLVFFIAAPEGADQTHLKLLAKLA 119

Query: 122 QYLLKDGFADKLRQVTNPDDVINLFNAT------EEEKKEATPAAPV------------- 162
           + L+K  F   LR   +  +V+ L +        EE    AT AA               
Sbjct: 120 RSLMKKDFTASLRAARSEQEVVRLVDGALGLGPAEEGPAGATSAAATPAAVAAGGDAAGA 179

Query: 163 ---------ADSHDFLVAVTACTTGIAHTYMAEEALKKQAAEMGVGIKVETNGASGVGNK 213
                    A     +VAVTAC TGIAHTYMA + L   A E+GV ++VET G++G   K
Sbjct: 180 AAPEQAPAAAGQRRRVVAVTACPTGIAHTYMAADGLSNAAQELGVDLQVETQGSAGF-TK 238

Query: 214 LTADDIKRAKGVIIAADKAV-EMDRFNGKPLISRPVAEGIKKPEELINIILDGKAE---- 268
           L    I  A  VI A D  V +  RF GKP ++ PV  GI +P+ +I   L  +AE    
Sbjct: 239 LDPAAIAAADAVIFATDVDVRDRGRFAGKPYVASPVKRGIDEPDVMIREAL-ARAEDPDA 297

Query: 269 AYVADNSDLSSEASSSEKAGLGSAFYKHLMSGVSQMLPFVIGGGIMIALSFLI------- 321
             V      + +A++S + G G+   K +M+GVS M+PFV  GG+++A  F++       
Sbjct: 298 PRVQGGGAGAEDAAASGQEGWGTRIRKAVMTGVSYMIPFVAAGGLLMAFGFMVAGADIAN 357

Query: 322 --DQFMGVPKSSLSHLGNY---HEIAAIFNQVGNAAFGFMIPVFAAYIAYSIAEKPGLVA 376
             D  +G   S+L +LG +     + A+  + GN A   ++   A YIAY +A++PG+  
Sbjct: 358 IADDVLGT--STLWNLGEFTLPQYLGAVLFKTGNLAMSLLVAALAGYIAYGLADRPGIAP 415

Query: 377 GFVAGSMATTGLAFNKVAFFEFGEKASQASLTGIPSGFLGALAGGFLAGGVILVLKKALA 436
           GF AG +A                         + +GFLG + GG LAG     L K   
Sbjct: 416 GFAAGLVANF-----------------------MGAGFLGGIVGGLLAGLAAYWLAKPQ- 451

Query: 437 FVPRSLEGIKSILLYPLLG-VLVTGFLMLFVNIPMAAINTALYNFLGNLSGGSAVLLGLI 495
            +PR +  +  +++ PLL  +   G L+L +  P+A     L   L  ++G  A+ LG I
Sbjct: 452 -LPRWVGSLMPVVIIPLLASIFAGGLLLLVLGGPIATFMAWLTEQLSGMTGAGALALGAI 510

Query: 496 VGGMMAIDMGGPFNKAAYVFGTSTLTAAALAKGG-SVVMASVMAGGMVPPLAVFVATLLF 554
           +G MM  D+GGP NK AY F  + L AA  A      +MA+V+A GMVPPL + +A+L+ 
Sbjct: 511 LGFMMGFDLGGPINKVAYTFAAAGLGAATAANTAPQEIMAAVIAAGMVPPLGLALASLVA 570

Query: 555 KNKFTQEEHDAGLTNIVMGLSFITEGAIPFGAGDPARAIPSFIVGSAVTGALVGLSGIKL 614
           K  F+  E + G    ++GLSFI+EGAIPF A DP R +P+ + G A  GA+   + +  
Sbjct: 571 KRYFSTVEQENGKAAWLLGLSFISEGAIPFAAADPLRVLPATMAGGAAAGAVAMGAAVTS 630

Query: 615 MAPHGGIFVIALTSNPLLYLLYIAVGAVIAGILFGSLRKV 654
            APHGG++++ +  NPL++L  + VG V+   +  +L+ V
Sbjct: 631 PAPHGGVWILPIIGNPLMFLAAVLVGTVVTAGVVVALKHV 670


Lambda     K      H
   0.320    0.137    0.381 

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: 1102
Number of extensions: 58
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: 655
Length of database: 694
Length adjustment: 39
Effective length of query: 616
Effective length of database: 655
Effective search space:   403480
Effective search space used:   403480
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: 54 (25.4 bits)

This GapMind analysis is from Sep 24 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