GapMind for catabolism of small carbon sources

 

Alignments for a candidate for deoD in Klebsiella michiganensis M5al

Align Purine nucleoside phosphorylase 2; Inosine-guanosine phosphorylase; Purine nucleoside phosphorylase II; PNP II; Xanthosine phosphorylase; EC 2.4.2.1 (characterized)
to candidate BWI76_RS20605 BWI76_RS20605 purine-nucleoside phosphorylase

Query= SwissProt::P45563
         (277 letters)



>FitnessBrowser__Koxy:BWI76_RS20605
          Length = 277

 Score =  493 bits (1268), Expect = e-144
 Identities = 245/277 (88%), Positives = 258/277 (93%)

Query: 1   MSQVQFSHNPLFCIDIIKTYKPDFTPRVAFILGSGLGALADQIENAVAISYEKLPGFPVS 60
           MS   FS NP +  DII+ YKPDFTPRVAFILGSGLGALA+QIE+AVAISYEKLPGFPVS
Sbjct: 1   MSDTLFSQNPWYSADIIRGYKPDFTPRVAFILGSGLGALAEQIEDAVAISYEKLPGFPVS 60

Query: 61  TVHGHAGELVLGHLQGVPVVCMKGRGHFYEGRGMTIMTDAIRTFKLLGCELLFCTNAAGS 120
           TVHGHAGELVLG+L GVPV CMKGRGHFYEGRGM +MTDAIRT KLLGCELLFCTNAAGS
Sbjct: 61  TVHGHAGELVLGNLAGVPVACMKGRGHFYEGRGMPVMTDAIRTLKLLGCELLFCTNAAGS 120

Query: 121 LRPEVGAGSLVALKDHINTMPGTPMVGLNDDRFGERFFSLANAYDAEYRALLQKVAKEEG 180
           LRPEVG GSLVAL DHINTMPGTPMVG ND+RFGERFFSLANAYDA+YRA+LQ VA EEG
Sbjct: 121 LRPEVGPGSLVALSDHINTMPGTPMVGPNDERFGERFFSLANAYDADYRAVLQSVAAEEG 180

Query: 181 FPLTEGVFVSYPGPNFETAAEIRMMQIIGGDVVGMSVVPEVISARHCDLKVVAVSAITNM 240
           FPLTEGVFVSYPGPNFETAAEIRMMQIIGGDVVGMSVVPEVI+ARHC LKVVAVSAITN+
Sbjct: 181 FPLTEGVFVSYPGPNFETAAEIRMMQIIGGDVVGMSVVPEVITARHCGLKVVAVSAITNL 240

Query: 241 AEGLSDVKLSHAQTLAAAELSKQNFINLICGFLRKIA 277
           AEGL DVKLSHAQTLAAAELS+QNFINLICGFLRK+A
Sbjct: 241 AEGLGDVKLSHAQTLAAAELSRQNFINLICGFLRKLA 277


Lambda     K      H
   0.323    0.139    0.410 

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: 393
Number of extensions: 5
Number of successful extensions: 1
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: 277
Length of database: 277
Length adjustment: 25
Effective length of query: 252
Effective length of database: 252
Effective search space:    63504
Effective search space used:    63504
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 bits)
S2: 47 (22.7 bits)

Align candidate BWI76_RS20605 BWI76_RS20605 (purine-nucleoside phosphorylase)
to HMM TIGR01699 (xapA: xanthosine phosphorylase (EC 2.4.2.1))

# hmmsearch :: search profile(s) against a sequence database
# HMMER 3.3.1 (Jul 2020); http://hmmer.org/
# Copyright (C) 2020 Howard Hughes Medical Institute.
# Freely distributed under the BSD open source license.
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
# query HMM file:                  ../tmp/path.carbon/TIGR01699.hmm
# target sequence database:        /tmp/gapView.22675.genome.faa
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -

Query:       TIGR01699  [M=248]
Accession:   TIGR01699
Description: XAPA: xanthosine phosphorylase
Scores for complete sequences (score includes all domains):
   --- full sequence ---   --- best 1 domain ---    -#dom-
    E-value  score  bias    E-value  score  bias    exp  N  Sequence                               Description
    ------- ------ -----    ------- ------ -----   ---- --  --------                               -----------
   1.3e-157  508.7   0.5   1.5e-157  508.5   0.5    1.0  1  lcl|FitnessBrowser__Koxy:BWI76_RS20605  BWI76_RS20605 purine-nucleoside 


Domain annotation for each sequence (and alignments):
>> lcl|FitnessBrowser__Koxy:BWI76_RS20605  BWI76_RS20605 purine-nucleoside phosphorylase
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  508.5   0.5  1.5e-157  1.5e-157       1     248 []      27     274 ..      27     274 .. 1.00

  Alignments for each domain:
  == domain 1  score: 508.5 bits;  conditional E-value: 1.5e-157
                               TIGR01699   1 rvafilgsglgdlvdqiendvaisyedlpgfpvssvhghagelvlgdlqgvpvvcmkgrghfyegkgmsim 71 
                                             rvafilgsglg+l++qie++vaisye+lpgfpvs+vhghagelvlg+l+gvpv cmkgrghfyeg+gm +m
  lcl|FitnessBrowser__Koxy:BWI76_RS20605  27 RVAFILGSGLGALAEQIEDAVAISYEKLPGFPVSTVHGHAGELVLGNLAGVPVACMKGRGHFYEGRGMPVM 97 
                                             79********************************************************************* PP

                               TIGR01699  72 tdavrtfkllgcellfctnaagslrpevlagslvalkdhintmpgtplvglnddrfgerffslanaydkel 142
                                             tda+rt+kllgcellfctnaagslrpev++gslval dhintmpgtp+vg+nd+rfgerffslanayd+++
  lcl|FitnessBrowser__Koxy:BWI76_RS20605  98 TDAIRTLKLLGCELLFCTNAAGSLRPEVGPGSLVALSDHINTMPGTPMVGPNDERFGERFFSLANAYDADY 168
                                             *********************************************************************** PP

                               TIGR01699 143 radlakvakeedipltegvfvsylgpnfetaaeirmmqiiggdvvgmsvvpevlsaahcdlkvvalsaitn 213
                                             ra l+ va ee++pltegvfvsy+gpnfetaaeirmmqiiggdvvgmsvvpev++a+hc+lkvva+saitn
  lcl|FitnessBrowser__Koxy:BWI76_RS20605 169 RAVLQSVAAEEGFPLTEGVFVSYPGPNFETAAEIRMMQIIGGDVVGMSVVPEVITARHCGLKVVAVSAITN 239
                                             *********************************************************************** PP

                               TIGR01699 214 laeglsdvklsheqtlkaaklakvnfiklieaflk 248
                                             laegl dvklsh+qtl+aa+l+++nfi+li++fl+
  lcl|FitnessBrowser__Koxy:BWI76_RS20605 240 LAEGLGDVKLSHAQTLAAAELSRQNFINLICGFLR 274
                                             *********************************97 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (248 nodes)
Target sequences:                          1  (277 residues searched)
Passed MSV filter:                         1  (1); expected 0.0 (0.02)
Passed bias filter:                        1  (1); expected 0.0 (0.02)
Passed Vit filter:                         1  (1); expected 0.0 (0.001)
Passed Fwd filter:                         1  (1); expected 0.0 (1e-05)
Initial search space (Z):                  1  [actual number of targets]
Domain search space  (domZ):               1  [number of targets reported over threshold]
# CPU time: 0.00u 0.00s 00:00:00.00 Elapsed: 00:00:00.00
# Mc/sec: 9.59
//
[ok]

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