Aligments for a candidate for iatA in Pseudomonas fluorescens FW300-N2E2

GapMind for catabolism of small carbon sources

Aligments for a candidate for iatA in Pseudomonas fluorescens FW300-N2E2

Align Inositol transport ATP-binding protein IatA, component of The myoinositol (high affinity)/ D-ribose (low affinity) transporter IatP/IatA/IbpA. The structure of IbpA with myoinositol bound has been solved (characterized)
to candidate Pf6N2E2_5969 L-arabinose transport ATP-binding protein AraG (TC 3.A.1.2.2)

Query= TCDB::B8H229
         (515 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_5969
          Length = 514

 Score =  377 bits (969), Expect = e-109
 Identities = 220/499 (44%), Positives = 314/499 (62%), Gaps = 10/499 (2%)

Query: 9   VSKSFPGVRALDQVDLVVGVGEVHALLGENGAGKSTLIKILSAAHAADAGTVTFAGQVLD 68
           + KSFPGV+AL  +  V   G+VHAL+GENGAGKSTL+KIL  A+   +G +    Q + 
Sbjct: 21  IGKSFPGVQALANISFVAHPGQVHALMGENGAGKSTLLKILGGAYIPSSGDLQIGEQTMA 80

Query: 69  PRDAPLRRQQLGIATIYQEFNLFPELSVAENMYLGREPRRLGLVDWSRLRADAQALLNDL 128
            +         G+A I+QE +L PE++VAEN++LG  P R GLV+   LR  A  LL  L
Sbjct: 81  FKGTADSIAS-GVAVIHQELHLVPEMTVAENLFLGHLPARFGLVNRGVLRQQALTLLKGL 139

Query: 129 GLPLNPDAPVRGLTVAEQQMVEIAKAMTLNARLIIMDEPTAALSGREVDRLHAIIAGLKA 188
              ++P   V  L++ ++Q+VEIAKA++  A +I  DEPT++LS RE+DRL AII  L+ 
Sbjct: 140 ADEIDPQEKVGRLSLGQRQLVEIAKALSRGAHVIAFDEPTSSLSAREIDRLMAIIGRLRD 199

Query: 189 RSVSVIYVSHRLGEVKAMCDRYTVMRDGRFVASGD-VADVEVADMVRLMVGRHVEFERRK 247
               V+YVSHR+ EV  +C+  TV +DGR+V + + ++++    +V  MVGR ++     
Sbjct: 200 EGKVVLYVSHRMEEVFRICNAVTVFKDGRYVRTFENMSELTHDQLVTCMVGRDIQDIYDY 259

Query: 248 RRRPPGAVVLKVEGVTPAAPRLSAPGYLRQVSFAARGGEIVGLAGLVGAGRTDLARLIFG 307
           R R  G V L+V+G       L  PG    VSF    GEI+GL GLVGAGRT+L RL+ G
Sbjct: 260 RPRERGDVALQVKG-------LLGPGLHEPVSFQVHKGEILGLFGLVGAGRTELLRLLSG 312

Query: 308 ADPIAAGRVLVDDKPLRLRSPRDAIQAGIMLVPEDRKQQGCFLDHSIRRNLSLPSLKALS 367
            +    G +++ DK L+LRSPRDAI AG++L PEDRK++G     S+  N+++ +  + S
Sbjct: 313 LERQREGSLVLHDKELKLRSPRDAIAAGVLLCPEDRKKEGIIPLGSVGENINISARPSHS 372

Query: 368 ALGQWVDERAERDLVETYRQKLRIKMADAETAIGKLSGGNQQKVLLGRAMALTPKVLIVD 427
            LG  +    ER   +   + L++K   A   I  LSGGNQQK +LGR +++  KVL++D
Sbjct: 373 TLGCLLRGDWERGNADKQIKSLKVKTPTAGQKIMYLSGGNQQKAILGRWLSMPMKVLLLD 432

Query: 428 EPTRGIDIGAKAEVHQVLSDLADLGVAVVVISSELAEVMAVSDRIVVFREGVIVADLDAQ 487
           EPTRGIDIGAKAE++Q++ +LA  G+AV+V+SS+L EVM +SDRI+V  EG +  +L   
Sbjct: 433 EPTRGIDIGAKAEIYQIIHNLAADGIAVIVVSSDLMEVMGISDRILVLCEGAMRGELSRD 492

Query: 488 TATEEGLMAYMATGTDRVA 506
            A E  L+  +A    RVA
Sbjct: 493 QANESNLL-QLALPRQRVA 510



 Score = 65.1 bits (157), Expect = 6e-15
 Identities = 60/220 (27%), Positives = 99/220 (45%), Gaps = 10/220 (4%)

Query: 5   DVSQVSKSFPGVRALDQVDLVVGVGEVHALLGENGAGKSTLIKILSAAHAADAGTVTFAG 64
           DV+   K   G    + V   V  GE+  L G  GAG++ L+++LS       G++    
Sbjct: 266 DVALQVKGLLGPGLHEPVSFQVHKGEILGLFGLVGAGRTELLRLLSGLERQREGSLVLHD 325

Query: 65  QVL---DPRDAPLRRQQLGIATIYQEFNLFPELSVAENMYLGREPRR--LGLV---DWSR 116
           + L    PRDA +    L      ++  + P  SV EN+ +   P    LG +   DW R
Sbjct: 326 KELKLRSPRDA-IAAGVLLCPEDRKKEGIIPLGSVGENINISARPSHSTLGCLLRGDWER 384

Query: 117 LRADAQALLNDLGLPLNPDAPVRGLTVAEQQMVEIAKAMTLNARLIIMDEPTAALSGREV 176
             AD Q     +  P      +  L+   QQ   + + +++  +++++DEPT  +     
Sbjct: 385 GNADKQIKSLKVKTP-TAGQKIMYLSGGNQQKAILGRWLSMPMKVLLLDEPTRGIDIGAK 443

Query: 177 DRLHAIIAGLKARSVSVIYVSHRLGEVKAMCDRYTVMRDG 216
             ++ II  L A  ++VI VS  L EV  + DR  V+ +G
Sbjct: 444 AEIYQIIHNLAADGIAVIVVSSDLMEVMGISDRILVLCEG 483


Lambda     K      H
   0.320    0.136    0.380 

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: 688
Number of extensions: 34
Number of successful extensions: 8
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: 515
Length of database: 514
Length adjustment: 35
Effective length of query: 480
Effective length of database: 479
Effective search space:   229920
Effective search space used:   229920
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