GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Skermanella stibiiresistens SB22

Align D-glucosaminate dehydratase (EC 4.3.1.9) (characterized)
to candidate WP_037460216.1 N825_RS30795 amino acid deaminase

Query= reanno::pseudo5_N2C3_1:AO356_00450
         (405 letters)



>NCBI__GCF_000576635.1:WP_037460216.1
          Length = 430

 Score =  312 bits (799), Expect = 1e-89
 Identities = 174/395 (44%), Positives = 240/395 (60%), Gaps = 10/395 (2%)

Query: 21  LLKDVSLPALVLHRAALEHNIRWMQAFVTDSGAELAPHGKTSMTPALFRRQLDAGAWGLT 80
           L +D++LP  VL  AAL HN +WM+ F+  +G  LAPHGKT+M+PALF RQL  GAWG+T
Sbjct: 36  LREDMTLPLAVLKDAALAHNGQWMRRFLDLTGTALAPHGKTTMSPALFDRQLSDGAWGMT 95

Query: 81  LATAVQTRAAYAHGVRRVLMANQLVGTPNMALIA-DLLADPAFEFHCMVDHPDNVADLGA 139
           LATA Q R A   G+RR+++AN LVG   +  +A +L +DP F+F C+VD  D V  L A
Sbjct: 96  LATAQQVRVAREAGIRRIVLANHLVGRQAIDYVAAELASDPDFDFFCLVDSIDGVERLLA 155

Query: 140 FF--ASRGMKLNVMIEYGVVGGRCGCRTEAEVLALAEAI-RSQPALALTGIEGYEGVIHG 196
                S G  L VM+E G  GGR GCR +A  L +A A+ R++P L L G+EGYEG++ G
Sbjct: 156 RLREVSPGRPLQVMVEIGAAGGRTGCRDDAGALEVARAVKRAEPLLTLRGVEGYEGMVRG 215

Query: 197 D---HAISGIRAFAASLVRLAVQLQDDDAFAIDKPIITASGSAWYDLIAESFEAQNAHGR 253
           D      + I A+   +V +A      D F     I++A GSA+YD++A+          
Sbjct: 216 DGDQDRDAAILAYLDRIVAVASDCAAADLFGPGPVILSAGGSAFYDMVADRLGKAKLDRE 275

Query: 254 FLSVLRPGSYVAHDHGIYKEAQCCVLERRSD---LHEGLRPALEVWAHVQSLPEPGFAVI 310
            L +LR G Y+ HD   Y      V  R  +   L  G   ALEVWA+VQS P+P   ++
Sbjct: 276 TLVLLRSGCYLTHDSDSYAVMFEQVRSRMPEVDGLGRGPAAALEVWAYVQSRPQPDKVIL 335

Query: 311 ALGKRDVAYDAGLPVPLKRYTPGSDSVPGDDVSGCKVTAVMDQHAFMSVAAGVELRVGDI 370
            +GKRD+++DAG+PVP+  + PG    P +   G  VT + DQHA +S+   V+LRVGD+
Sbjct: 336 TVGKRDISHDAGMPVPILWFRPGHHGAPVEAPRGLVVTELNDQHAHVSIPERVDLRVGDM 395

Query: 371 IAFGTSHPCLTFDKWRVGCLVDEQLRVVESMETCF 405
           +A G SHPC TFDKWRV  +VD++  +V ++ T F
Sbjct: 396 VALGISHPCTTFDKWRVLYVVDDRYDIVSAVTTWF 430


Lambda     K      H
   0.322    0.136    0.414 

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: 486
Number of extensions: 18
Number of successful extensions: 6
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: 405
Length of database: 430
Length adjustment: 32
Effective length of query: 373
Effective length of database: 398
Effective search space:   148454
Effective search space used:   148454
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 24 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