GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rbsA in Alkalihalobacterium alkalinitrilicum DSM 22532

Align Ribose import ATP-binding protein RbsA 2, component of D-ribose porter (Nanavati et al., 2006). Induced by ribose (characterized)
to candidate WP_078427103.1 BK574_RS00955 ABC transporter ATP-binding protein

Query= TCDB::Q9X051
         (523 letters)



>NCBI__GCF_002019605.1:WP_078427103.1
          Length = 509

 Score =  323 bits (828), Expect = 9e-93
 Identities = 184/494 (37%), Positives = 290/494 (58%), Gaps = 4/494 (0%)

Query: 12  LLEARNITKTFPGVIAVNNVTLQIYKGEVCALVGENGAGKSTLMKILAGVYPDYEGQIFL 71
           ++E ++I K FPG++A +NVTLQ+ +GE+ AL+GENGAGKSTLM +L G+Y   +G+I +
Sbjct: 4   VIEMKDIRKEFPGIVANDNVTLQVKQGEIHALLGENGAGKSTLMNVLFGLYQPEKGEILV 63

Query: 72  EGKEVRFRNPREAQENGIALIPQELDLVPNLSSAENIFLSREPVNEFGVIEYQKMFEQAS 131
           +GK V+  +P  A   GI ++ Q   LV   +  ENI L +EP    G I  +K  +   
Sbjct: 64  KGKPVKITDPNVANRLGIGMVHQHFMLVEKFTVTENIILGKEPTAG-GKINIKKAAKAVE 122

Query: 132 KLFSKLGVNIDPKTKVEDLSTSQQQMVAIAKALSLDAKIIIMDEPTSAIGKRETEQLFNI 191
            +  + G+ +DP  K++D+S   QQ V I K L   A+I+I DEPT+A+  +E  +L  I
Sbjct: 123 TISKQYGLAVDPYAKIQDISVGMQQRVEILKTLYRGAEILIFDEPTAALTPQEITELIQI 182

Query: 192 IRSLKNEGKSVIYISHRLEEIFEIADRVVVMRDGRKVGEGPIEEFDHDKLVRLMVGRSID 251
           ++ L +EGKS+I I+H+L+EI E+ DR  V+R GR +G   I E   D L  +MVGR ++
Sbjct: 183 MKKLVSEGKSIILITHKLKEIMEVCDRCTVIRRGRGIGTVDISESTPDSLAAMMVGREVN 242

Query: 252 QFFIKERATITDEIFRVEGIKLWSLDRKKLLVDDVSFYVRKGEVLGIYGLVGAGRTELLE 311
               K+ A   D + +++ + +    R    V+D+   V  GE+LG+ G+ G G+TEL+E
Sbjct: 243 FSVEKDPAQPKDAVLQIKDLVVKD-SRDITAVNDLHLEVHAGEILGVAGVDGNGQTELIE 301

Query: 312 AIFGAHPGRTEGKVFIGGKEIKIHSPRDAVKNGIGLVPEDRKTAGLILQMSVLHNITLPS 371
           AI G     T G + + G++I   +PR     G+G +P+DR   GL+L  +V  NI L +
Sbjct: 302 AITGLRK-PTGGNIQLNGQDITGLTPRKITGAGVGHIPQDRHKHGLVLDFTVGENIVLQT 360

Query: 372 VVMKLIVRKFGLIDSQLEKEIVRSFIEKLNIKTPSPYQIVENLSGGNQQKVVLAKWLAIK 431
              K       L  +++ K+     IE  +++TPS + +   LSGGNQQK ++A+ +   
Sbjct: 361 YYQKPYSTSGVLNFNEIYKK-ANELIEDYDVRTPSEHTLARALSGGNQQKAIIAREVDRS 419

Query: 432 PKVLLLDEPTRGIDVNAKSEIYKLISEMAVSGMGVVMVSSELPEILAMSDRILVMSEGRK 491
           P +L+  +PTRG+DV A   I+  + +    G  V+++S EL E+L +SDRI V+ EG+ 
Sbjct: 420 PDLLIAAQPTRGLDVGAIESIHHRLVKERDKGKAVLLISLELDEVLNVSDRIAVIYEGKI 479

Query: 492 TAEFLREEVTEEDL 505
            A    ++  E +L
Sbjct: 480 VAIVDADKTNENEL 493



 Score =  100 bits (248), Expect = 2e-25
 Identities = 63/249 (25%), Positives = 133/249 (53%), Gaps = 8/249 (3%)

Query: 9   REVLLEARN-ITKTFPGVIAVNNVTLQIYKGEVCALVGENGAGKSTLMKILAGVYPDYEG 67
           ++ +L+ ++ + K    + AVN++ L+++ GE+  + G +G G++ L++ + G+     G
Sbjct: 253 KDAVLQIKDLVVKDSRDITAVNDLHLEVHAGEILGVAGVDGNGQTELIEAITGLRKPTGG 312

Query: 68  QIFLEGKEVRFRNPREAQENGIALIPQELD---LVPNLSSAENIFLS---REPVNEFGVI 121
            I L G+++    PR+    G+  IPQ+     LV + +  ENI L    ++P +  GV+
Sbjct: 313 NIQLNGQDITGLTPRKITGAGVGHIPQDRHKHGLVLDFTVGENIVLQTYYQKPYSTSGVL 372

Query: 122 EYQKMFEQASKLFSKLGVNIDPK-TKVEDLSTSQQQMVAIAKALSLDAKIIIMDEPTSAI 180
            + +++++A++L     V    + T    LS   QQ   IA+ +     ++I  +PT  +
Sbjct: 373 NFNEIYKKANELIEDYDVRTPSEHTLARALSGGNQQKAIIAREVDRSPDLLIAAQPTRGL 432

Query: 181 GKRETEQLFNIIRSLKNEGKSVIYISHRLEEIFEIADRVVVMRDGRKVGEGPIEEFDHDK 240
                E + + +   +++GK+V+ IS  L+E+  ++DR+ V+ +G+ V     ++ + ++
Sbjct: 433 DVGAIESIHHRLVKERDKGKAVLLISLELDEVLNVSDRIAVIYEGKIVAIVDADKTNENE 492

Query: 241 LVRLMVGRS 249
           L  LM G S
Sbjct: 493 LGLLMAGGS 501



 Score = 92.4 bits (228), Expect = 3e-23
 Identities = 61/234 (26%), Positives = 118/234 (50%), Gaps = 16/234 (6%)

Query: 284 DDVSFYVRKGEVLGIYGLVGAGRTELLEAIFGAHPGRTEGKVFIGGKEIKIHSPRDAVKN 343
           D+V+  V++GE+  + G  GAG++ L+  +FG +    +G++ + GK +KI  P  A + 
Sbjct: 21  DNVTLQVKQGEIHALLGENGAGKSTLMNVLFGLYQPE-KGEILVKGKPVKITDPNVANRL 79

Query: 344 GIGLVPEDRKTAGLILQMSVLHNITL---PSVVMKLIVRKFGLIDSQLEKEIVRSFIEKL 400
           GIG+V +      L+ + +V  NI L   P+   K+ ++K       + K+   +     
Sbjct: 80  GIGMVHQHFM---LVEKFTVTENIILGKEPTAGGKINIKKAAKAVETISKQYGLAV---- 132

Query: 401 NIKTPSPYQIVENLSGGNQQKVVLAKWLAIKPKVLLLDEPTRGIDVNAKSEIYKLISEMA 460
                 PY  ++++S G QQ+V + K L    ++L+ DEPT  +     +E+ +++ ++ 
Sbjct: 133 -----DPYAKIQDISVGMQQRVEILKTLYRGAEILIFDEPTAALTPQEITELIQIMKKLV 187

Query: 461 VSGMGVVMVSSELPEILAMSDRILVMSEGRKTAEFLREEVTEEDLLKAAIPRSV 514
             G  +++++ +L EI+ + DR  V+  GR        E T + L    + R V
Sbjct: 188 SEGKSIILITHKLKEIMEVCDRCTVIRRGRGIGTVDISESTPDSLAAMMVGREV 241


Lambda     K      H
   0.317    0.137    0.372 

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: 643
Number of extensions: 37
Number of successful extensions: 12
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 4
Number of HSP's successfully gapped: 3
Length of query: 523
Length of database: 509
Length adjustment: 35
Effective length of query: 488
Effective length of database: 474
Effective search space:   231312
Effective search space used:   231312
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. 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