Alignments for a candidate for fruI in Maridesulfovibrio zosterae DSM 11974

GapMind for catabolism of small carbon sources

Alignments for a candidate for fruI in Maridesulfovibrio zosterae DSM 11974

Align Multiphosphoryl transfer protein; MTP; Triphosphoryl transfer protein; TTP; EC 2.7.3.9 (characterized)
to candidate WP_027722339.1 H589_RS0112545 phosphoenolpyruvate--protein phosphotransferase

Query= SwissProt::P45597
         (838 letters)



>NCBI__GCF_000425265.1:WP_027722339.1
          Length = 829

 Score =  420 bits (1079), Expect = e-121
 Identities = 264/672 (39%), Positives = 383/672 (56%), Gaps = 29/672 (4%)

Query: 173 GLHARPATRWAETARGFSARAQVRAGDQAADAKSLVGLLQLGLRAGDSITVSAKGSDAPA 232
           GLHARPA     TA  F +   +R G  +A AKS+  +  L ++ GD+IT+S  G+DA  
Sbjct: 171 GLHARPAANLVSTAGKFKSSVAIRKGADSASAKSINQVALLSVKNGDTITISVSGADAQE 230

Query: 233 LLKRL-RAVMDSLTAQEKADAERAAQRRAAPVIGWTPPQAQPAIVGIGASPGVAIGIVHR 291
               L +   D+   +++  AE     +  PV+          IVG   S G A+G  + 
Sbjct: 231 AFDALIKLHKDNFGERDEDVAELVEDIK--PVV----QAGDGTIVGAPGSGGYAVGTAYV 284

Query: 292 LRAAQTEVADQPIGLGDGGVLLHD-ALTRTRQQLAAIQDDTQRRLGASDAAIFKAQAELL 350
            +A   EV  + I   +  +   D A++     +  +Q +T++  G ++AAIF+  A ++
Sbjct: 285 HQATLPEVERKNISDVETELEKLDLAISTALSDIKILQRETEKTSGKANAAIFEVHAMII 344

Query: 351 NDTDLITRTCQLMVEGH-GVAWSWHQAVEQIASGLAALGNPVLAGRAADLRDVGRRVLAQ 409
           +D D+  +  +++ E      ++W + + +I +    L +  +  RAAD+ D G RVL  
Sbjct: 345 SDKDMRDKAAEIVSEQQINADYAWFEVMNKITADYRNLDDTYMQARAADVMDCGGRVLRI 404

Query: 410 LDPAAAGAGLTDLP-EQPCILLAGDLSPSDTANLDTDCVLGLATAQGGPTSHTAILSRTL 468
           L    AG     +  E   I++A DLSPSD A LD + VLG+ T  GG TSH AILSR++
Sbjct: 405 L----AGEEEQGICLENGAIIVAHDLSPSDVAGLDLEKVLGVVTEIGGVTSHAAILSRSM 460

Query: 469 GLPALVAAGGQLLDIEDGVTAIIDGSSGRLYINPSELDLDAARTHIAEQQAI----RERE 524
           G+PA++ AG  +  I++G    ++G  G ++  P +    +    IAE++ +    RE  
Sbjct: 461 GIPAVIGAGKSIQQIQNGTIIALNGFEGVIWPEPEQ----SVVNDIAEKRVLWLAEREEA 516

Query: 525 AAQRALPAETTDGHHIDIGANVNLPEQVAMALTQGAEGVGLMRTEFLFLERGSTPTEDEQ 584
            A+ A PA+T DG  I +  N+ +P         GAEGVGL RTEFLF +R   PTEDEQ
Sbjct: 517 KAKGAAPAKTLDGTDIMVMGNIGVPADAPRVFEYGAEGVGLFRTEFLFQDRSQAPTEDEQ 576

Query: 585 YQTYLAMARALDGRPLIVRALDIGGDKQVAHLELPHEENPFLGVRGARLLLRRPDLLEPQ 644
           +  Y+  ARA+ G P+I+R LDIGGDK V +L+ P E+NPFLG RG R  + RP+L   Q
Sbjct: 577 FDAYVEAARAMQGNPVIIRTLDIGGDKPVKYLDTPEEDNPFLGERGIRFCMARPELFRTQ 636

Query: 645 LRALYRAAKDGARLSIMFPMITSVPELISLREICARIRAEL------DAPELPIGIMIEV 698
           LRAL RAA +   + IM+PMI+ V EL S+ EI  + R  L       A ++  GIMIEV
Sbjct: 637 LRALLRAASE-ENIWIMYPMISDVDELSSVLEIQNQAREVLVSEGVKIAEKIKTGIMIEV 695

Query: 699 PAAAAQADVLARHADFFSIGTNDLTQYVLAIDRQNPELAAEADSLHPAVLRMIRSTIDGA 758
           PAA A AD LA+  DFFSIGTNDLTQYV+A DR N  ++   D+L+PAVLRM+  T D A
Sbjct: 696 PAAVAVADKLAQKCDFFSIGTNDLTQYVMAADRGNASVSKLCDNLNPAVLRMVAMTCDAA 755

Query: 759 RKHDRWVGVCGGLAGDPFGASLLAGLGVQELSMTPNDIPAVKARLRGRALSALQQLAEQA 818
           +K    VG+CG LAG+   ++LL GLG+ ELSM    IP VK  +R   +   + LA++ 
Sbjct: 756 KKAGIEVGMCGELAGNSKASALLLGLGLDELSMNGPAIPEVKEAIRSVNMDDCRALAQKV 815

Query: 819 LQCETAEQVRAL 830
           L+  ++++VR L
Sbjct: 816 LEANSSDEVRDL 827


Lambda     K      H
   0.318    0.134    0.385 

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: 1318
Number of extensions: 46
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: 838
Length of database: 829
Length adjustment: 42
Effective length of query: 796
Effective length of database: 787
Effective search space:   626452
Effective search space used:   626452
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 (21.7 bits)
S2: 56 (26.2 bits)

This GapMind analysis is from Apr 09 2024. 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 2024 update 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