GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Klebsiella michiganensis M5al

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate BWI76_RS08385 BWI76_RS08385 citrate (Si)-synthase

Query= reanno::pseudo6_N2E2:Pf6N2E2_6062
         (375 letters)



>FitnessBrowser__Koxy:BWI76_RS08385
          Length = 427

 Score =  196 bits (499), Expect = 8e-55
 Identities = 132/366 (36%), Positives = 191/366 (52%), Gaps = 39/366 (10%)

Query: 32  LTYRGYDVRDLAADAQFEEVAYLLLYGELPTQAQLDAYTGKLRQLRDLPQALKEVLERIP 91
           L +RG+ +  LA D+ + EV Y+LL GE PTQAQ D +   + +   + + +  +     
Sbjct: 67  LLHRGFPIDQLATDSNYLEVCYILLNGEKPTQAQYDEFKTIVTRHTMIHEQITRLFHAFR 126

Query: 92  ADAHPMDVMRTGCSFLGNLEPEQDFSQQHDKTD------------RLLAAFP--AIMCYW 137
            D+HPM VM   C   G L      +  HD  D            RLL+  P  A MCY 
Sbjct: 127 RDSHPMAVM---CGITGALA-----AFYHDSLDVNNPRHRDIAAFRLLSKMPTMAAMCYK 178

Query: 138 YRFSHQGQRIECVTDEVSIGGHFLHLLHGKKPSELHV-----KVMNVSLILYAEHEFNAS 192
           Y     GQ      +++S  G+FL+++      +  V     + M+  LIL+A+HE NAS
Sbjct: 179 YSI---GQPFVYPRNDLSYAGNFLNMMFSTPCEKYEVNPILERAMDRILILHADHEQNAS 235

Query: 193 TFTARVCASTLSDLFSCITAAIGSLRGPLHGGANEAAMEMIERFSSPQEAIEGTLGMLAR 252
           T T R   S+ ++ F+CI A I SL GP HGGANEAA++M+E  SS +   E       +
Sbjct: 236 TSTVRTAGSSGANPFACIAAGIASLWGPAHGGANEAALKMLEEISSVEHIPEFVRRAKDK 295

Query: 253 KD--KIMGFGHAIYKDNDPRNEVIKGWSKKLADEVG--DTVLFPVSE----AIDKTMWEQ 304
            D  ++MGFGH +YK+ DPR  V++    ++  E+G  D +L    E    A++   + +
Sbjct: 296 NDSFRLMGFGHRVYKNYDPRATVMRETCHEVLKELGTKDDLLEVAMELEHIALNDPYFIE 355

Query: 305 KKLFPNADFYHASAYHFMGIPTKLFTPIFVCSRLTGWAAHVFEQRANN-RIIRPSAEYTG 363
           KKL+PN DFY       MGIP+ +FT IF  +R  GW AH  E  ++  +I RP   YTG
Sbjct: 356 KKLYPNVDFYSGIILKAMGIPSSMFTVIFAMARTVGWIAHWNEMHSDGMKIARPRQLYTG 415

Query: 364 VEQRKF 369
            E+R F
Sbjct: 416 YEKRDF 421


Lambda     K      H
   0.321    0.135    0.406 

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: 392
Number of extensions: 24
Number of successful extensions: 5
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: 375
Length of database: 427
Length adjustment: 31
Effective length of query: 344
Effective length of database: 396
Effective search space:   136224
Effective search space used:   136224
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 (21.9 bits)
S2: 50 (23.9 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:

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