Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H7J4
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 2 |
GO:0006520 | amino acid metabolic process | 3 | 2 |
GO:0006566 | threonine metabolic process | 6 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008652 | amino acid biosynthetic process | 4 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009066 | aspartate family amino acid metabolic process | 5 | 2 |
GO:0009067 | aspartate family amino acid biosynthetic process | 6 | 2 |
GO:0009088 | threonine biosynthetic process | 7 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016053 | organic acid biosynthetic process | 4 | 2 |
GO:0019752 | carboxylic acid metabolic process | 5 | 2 |
GO:0043436 | oxoacid metabolic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 2 |
GO:0044283 | small molecule biosynthetic process | 3 | 2 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
GO:1901605 | alpha-amino acid metabolic process | 4 | 2 |
GO:1901607 | alpha-amino acid biosynthetic process | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004795 | threonine synthase activity | 5 | 9 |
GO:0016829 | lyase activity | 2 | 9 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 9 |
GO:0016838 | carbon-oxygen lyase activity, acting on phosphates | 4 | 9 |
GO:0005488 | binding | 1 | 2 |
GO:0019842 | vitamin binding | 3 | 2 |
GO:0030170 | pyridoxal phosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0070279 | vitamin B6 binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.447 |
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.623 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.344 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.224 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.193 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 531 | 533 | PF00082 | 0.193 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.571 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.403 |
DEG_SPOP_SBC_1 | 459 | 463 | PF00917 | 0.330 |
DOC_CKS1_1 | 196 | 201 | PF01111 | 0.333 |
DOC_CYCLIN_RxL_1 | 340 | 349 | PF00134 | 0.291 |
DOC_CYCLIN_RxL_1 | 470 | 482 | PF00134 | 0.265 |
DOC_MAPK_MEF2A_6 | 15 | 22 | PF00069 | 0.251 |
DOC_PP2B_PxIxI_1 | 463 | 469 | PF00149 | 0.250 |
DOC_PP4_FxxP_1 | 226 | 229 | PF00568 | 0.558 |
DOC_PP4_FxxP_1 | 242 | 245 | PF00568 | 0.250 |
DOC_PP4_FxxP_1 | 400 | 403 | PF00568 | 0.291 |
DOC_PP4_FxxP_1 | 502 | 505 | PF00568 | 0.392 |
DOC_PP4_FxxP_1 | 593 | 596 | PF00568 | 0.364 |
DOC_SPAK_OSR1_1 | 431 | 435 | PF12202 | 0.167 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.237 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.263 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.504 |
DOC_USP7_UBL2_3 | 631 | 635 | PF12436 | 0.446 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.271 |
LIG_14-3-3_CanoR_1 | 185 | 194 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 222 | 227 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 263 | 273 | PF00244 | 0.167 |
LIG_14-3-3_CanoR_1 | 364 | 373 | PF00244 | 0.247 |
LIG_14-3-3_CanoR_1 | 454 | 459 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 509 | 513 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 65 | 74 | PF00244 | 0.398 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.595 |
LIG_BRCT_BRCA1_1 | 99 | 103 | PF00533 | 0.511 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.385 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.365 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.425 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.413 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.345 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.345 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.448 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.451 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.241 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.250 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.330 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.598 |
LIG_GBD_Chelix_1 | 488 | 496 | PF00786 | 0.392 |
LIG_LIR_Apic_2 | 223 | 229 | PF02991 | 0.536 |
LIG_LIR_Apic_2 | 240 | 245 | PF02991 | 0.151 |
LIG_LIR_Gen_1 | 112 | 123 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 271 | 278 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 440 | 451 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 475 | 481 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 587 | 598 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 271 | 276 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 440 | 446 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 475 | 480 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 587 | 593 | PF02991 | 0.322 |
LIG_LYPXL_S_1 | 175 | 179 | PF13949 | 0.392 |
LIG_LYPXL_yS_3 | 176 | 179 | PF13949 | 0.392 |
LIG_PCNA_yPIPBox_3 | 231 | 242 | PF02747 | 0.442 |
LIG_PCNA_yPIPBox_3 | 339 | 352 | PF02747 | 0.278 |
LIG_PCNA_yPIPBox_3 | 439 | 447 | PF02747 | 0.392 |
LIG_PCNA_yPIPBox_3 | 65 | 78 | PF02747 | 0.389 |
LIG_Pex14_2 | 257 | 261 | PF04695 | 0.250 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.330 |
LIG_SH2_PTP2 | 273 | 276 | PF00017 | 0.284 |
LIG_SH2_SRC | 154 | 157 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.223 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.250 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.276 |
LIG_SH3_1 | 133 | 139 | PF00018 | 0.392 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.327 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.335 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.250 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.330 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.384 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.137 |
LIG_SUMO_SIM_anti_2 | 298 | 304 | PF11976 | 0.266 |
LIG_SUMO_SIM_anti_2 | 3 | 8 | PF11976 | 0.220 |
LIG_SUMO_SIM_anti_2 | 402 | 408 | PF11976 | 0.309 |
LIG_SUMO_SIM_anti_2 | 465 | 470 | PF11976 | 0.250 |
LIG_SUMO_SIM_par_1 | 158 | 163 | PF11976 | 0.167 |
LIG_SUMO_SIM_par_1 | 456 | 463 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 580 | 587 | PF11976 | 0.322 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.167 |
LIG_TRAF2_1 | 618 | 621 | PF00917 | 0.530 |
LIG_TYR_ITIM | 441 | 446 | PF00017 | 0.343 |
LIG_TYR_ITSM | 172 | 179 | PF00017 | 0.330 |
LIG_WRC_WIRS_1 | 317 | 322 | PF05994 | 0.392 |
MOD_CDK_SPxxK_3 | 195 | 202 | PF00069 | 0.244 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.349 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.420 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.267 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.250 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.418 |
MOD_CK1_1 | 537 | 543 | PF00069 | 0.386 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.636 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.479 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.361 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.241 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.330 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.286 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.358 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.633 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.264 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.271 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.516 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.250 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.384 |
MOD_GlcNHglycan | 50 | 54 | PF01048 | 0.480 |
MOD_GlcNHglycan | 535 | 539 | PF01048 | 0.305 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.484 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.403 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.360 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.275 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.348 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.371 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.562 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.563 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.270 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.411 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.250 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.263 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.333 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.441 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.462 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.364 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.506 |
MOD_LATS_1 | 82 | 88 | PF00433 | 0.278 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.370 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.305 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.179 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.366 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.262 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.273 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.250 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.245 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.263 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.410 |
MOD_NEK2_2 | 338 | 343 | PF00069 | 0.250 |
MOD_NEK2_2 | 526 | 531 | PF00069 | 0.284 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.250 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.392 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.392 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.367 |
MOD_PKA_1 | 97 | 103 | PF00069 | 0.501 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.396 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.179 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.230 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.348 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.280 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.468 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.445 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.262 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.328 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.360 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.400 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.379 |
MOD_Plk_1 | 565 | 571 | PF00069 | 0.443 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.270 |
MOD_Plk_2-3 | 70 | 76 | PF00069 | 0.250 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.165 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.401 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.339 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.376 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.330 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.327 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.271 |
MOD_SUMO_rev_2 | 11 | 16 | PF00179 | 0.472 |
TRG_DiLeu_BaEn_2 | 110 | 116 | PF01217 | 0.328 |
TRG_DiLeu_BaEn_4 | 111 | 117 | PF01217 | 0.167 |
TRG_DiLeu_BaLyEn_6 | 196 | 201 | PF01217 | 0.377 |
TRG_DiLeu_BaLyEn_6 | 372 | 377 | PF01217 | 0.275 |
TRG_DiLeu_BaLyEn_6 | 538 | 543 | PF01217 | 0.289 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.249 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.340 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.253 |
TRG_ER_diArg_1 | 429 | 431 | PF00400 | 0.167 |
TRG_ER_diArg_1 | 453 | 456 | PF00400 | 0.284 |
TRG_Pf-PMV_PEXEL_1 | 375 | 379 | PF00026 | 0.265 |
TRG_Pf-PMV_PEXEL_1 | 623 | 628 | PF00026 | 0.349 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZJ2 | Leptomonas seymouri | 71% | 99% |
A0A0S4ITY7 | Bodo saltans | 45% | 100% |
A0A1X0NNP4 | Trypanosomatidae | 48% | 100% |
A0A3Q8II85 | Leishmania donovani | 85% | 100% |
A0A422NX69 | Trypanosoma rangeli | 52% | 100% |
A4HVX7 | Leishmania infantum | 85% | 100% |
C9ZT46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9APM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
O24924 | Helicobacter pylori (strain ATCC 700392 / 26695) | 31% | 100% |
P16120 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
P23669 | Corynebacterium glutamicum (strain ATCC 13032 / DSM 20300 / BCRC 11384 / JCM 1318 / LMG 3730 / NCIMB 10025) | 34% | 100% |
P29363 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 33% | 100% |
P37145 | Methylobacillus glycogenes | 32% | 100% |
Q00063 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 30% | 100% |
Q2YDP8 | Danio rerio | 27% | 100% |
Q42598 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
Q4QFV0 | Leishmania major | 84% | 100% |
Q5M7T9 | Rattus norvegicus | 30% | 100% |
Q5R5P3 | Pongo abelii | 36% | 91% |
Q5RFE6 | Pongo abelii | 29% | 100% |
Q5XH07 | Xenopus laevis | 28% | 100% |
Q80W22 | Mus musculus | 29% | 100% |
Q86YJ6 | Homo sapiens | 29% | 100% |
Q8BH55 | Mus musculus | 37% | 90% |
Q8IYQ7 | Homo sapiens | 35% | 91% |
Q9BH05 | Macaca fascicularis | 35% | 91% |
V5BD69 | Trypanosoma cruzi | 48% | 100% |