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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AH29
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 486 | 488 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.422 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.740 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.515 |
CLV_PCSK_PC7_1 | 341 | 347 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.404 |
DEG_APCC_DBOX_1 | 176 | 184 | PF00400 | 0.545 |
DEG_APCC_DBOX_1 | 389 | 397 | PF00400 | 0.349 |
DEG_SPOP_SBC_1 | 135 | 139 | PF00917 | 0.503 |
DEG_SPOP_SBC_1 | 85 | 89 | PF00917 | 0.593 |
DOC_CDC14_PxL_1 | 434 | 442 | PF14671 | 0.314 |
DOC_CYCLIN_yCln2_LP_2 | 100 | 106 | PF00134 | 0.358 |
DOC_CYCLIN_yCln2_LP_2 | 124 | 127 | PF00134 | 0.305 |
DOC_CYCLIN_yCln2_LP_2 | 62 | 68 | PF00134 | 0.525 |
DOC_MAPK_gen_1 | 189 | 196 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 262 | 271 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 348 | 357 | PF00069 | 0.314 |
DOC_MAPK_gen_1 | 427 | 437 | PF00069 | 0.289 |
DOC_MAPK_gen_1 | 463 | 470 | PF00069 | 0.415 |
DOC_MAPK_MEF2A_6 | 348 | 356 | PF00069 | 0.271 |
DOC_PP2B_LxvP_1 | 124 | 127 | PF13499 | 0.305 |
DOC_PP2B_LxvP_1 | 507 | 510 | PF13499 | 0.391 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.538 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.509 |
DOC_USP7_UBL2_3 | 30 | 34 | PF12436 | 0.453 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.450 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 262 | 272 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 309 | 316 | PF00244 | 0.341 |
LIG_Actin_WH2_2 | 326 | 343 | PF00022 | 0.271 |
LIG_Actin_WH2_2 | 482 | 498 | PF00022 | 0.409 |
LIG_Actin_WH2_2 | 512 | 529 | PF00022 | 0.484 |
LIG_BRCT_BRCA1_1 | 316 | 320 | PF00533 | 0.414 |
LIG_deltaCOP1_diTrp_1 | 446 | 453 | PF00928 | 0.371 |
LIG_EH1_1 | 262 | 270 | PF00400 | 0.488 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.370 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.363 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.324 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.270 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.402 |
LIG_LIR_Apic_2 | 433 | 439 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 21 | 27 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 450 | 459 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 78 | 85 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 314 | 318 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 450 | 456 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.504 |
LIG_MYND_1 | 163 | 167 | PF01753 | 0.424 |
LIG_MYND_1 | 99 | 103 | PF01753 | 0.358 |
LIG_NRBOX | 113 | 119 | PF00104 | 0.537 |
LIG_NRBOX | 392 | 398 | PF00104 | 0.271 |
LIG_PCNA_yPIPBox_3 | 427 | 435 | PF02747 | 0.335 |
LIG_PCNA_yPIPBox_3 | 483 | 496 | PF02747 | 0.474 |
LIG_Pex14_1 | 448 | 452 | PF04695 | 0.371 |
LIG_Pex14_1 | 77 | 81 | PF04695 | 0.402 |
LIG_Pex14_2 | 452 | 456 | PF04695 | 0.362 |
LIG_REV1ctd_RIR_1 | 450 | 459 | PF16727 | 0.413 |
LIG_SH2_CRK | 81 | 85 | PF00017 | 0.433 |
LIG_SH2_NCK_1 | 81 | 85 | PF00017 | 0.410 |
LIG_SH2_PTP2 | 436 | 439 | PF00017 | 0.289 |
LIG_SH2_SRC | 436 | 439 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 81 | 85 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.393 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.615 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.428 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.349 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.475 |
LIG_SUMO_SIM_anti_2 | 110 | 116 | PF11976 | 0.381 |
LIG_SUMO_SIM_anti_2 | 358 | 364 | PF11976 | 0.284 |
LIG_SUMO_SIM_par_1 | 353 | 359 | PF11976 | 0.289 |
LIG_SUMO_SIM_par_1 | 465 | 472 | PF11976 | 0.361 |
LIG_TYR_ITIM | 79 | 84 | PF00017 | 0.425 |
LIG_UBA3_1 | 22 | 30 | PF00899 | 0.402 |
LIG_WRC_WIRS_1 | 38 | 43 | PF05994 | 0.439 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.512 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.640 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.489 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.350 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.491 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.540 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.550 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.678 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.532 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.385 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.591 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.303 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.306 |
MOD_GlcNHglycan | 405 | 409 | PF01048 | 0.379 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.484 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.545 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.454 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.516 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.668 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.508 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.499 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.398 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.527 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.332 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.370 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.483 |
MOD_LATS_1 | 241 | 247 | PF00433 | 0.688 |
MOD_N-GLC_2 | 211 | 213 | PF02516 | 0.598 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.426 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.232 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.560 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.644 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.549 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.525 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.388 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.297 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.430 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.392 |
MOD_NEK2_2 | 18 | 23 | PF00069 | 0.426 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.429 |
MOD_PIKK_1 | 245 | 251 | PF00454 | 0.663 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.270 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.372 |
MOD_PK_1 | 102 | 108 | PF00069 | 0.485 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.339 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.412 |
MOD_PKB_1 | 262 | 270 | PF00069 | 0.488 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.396 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.335 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.429 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.418 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.364 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.371 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.289 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.377 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.449 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.618 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.523 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.363 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.441 |
TRG_DiLeu_BaEn_2 | 18 | 24 | PF01217 | 0.352 |
TRG_DiLeu_BaEn_2 | 233 | 239 | PF01217 | 0.665 |
TRG_DiLeu_BaLyEn_6 | 175 | 180 | PF01217 | 0.523 |
TRG_DiLeu_BaLyEn_6 | 96 | 101 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 261 | 264 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 344 | 346 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 390 | 392 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 526 | 528 | PF00400 | 0.412 |
TRG_NES_CRM1_1 | 206 | 217 | PF08389 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 15 | 19 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 169 | 173 | PF00026 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 331 | 335 | PF00026 | 0.271 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTJ8 | Leptomonas seymouri | 63% | 100% |
A0A1X0NKH8 | Trypanosomatidae | 37% | 100% |
A0A3Q8IG04 | Leishmania donovani | 99% | 100% |
A0A3R7MBQ6 | Trypanosoma rangeli | 37% | 100% |
A4HD75 | Leishmania braziliensis | 84% | 100% |
D0A6Y7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 99% |
E9AWK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QAW3 | Leishmania major | 93% | 100% |
V5BRB9 | Trypanosoma cruzi | 37% | 100% |