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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3Q8II15
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 426 | 430 | PF00656 | 0.655 |
CLV_MEL_PAP_1 | 61 | 67 | PF00089 | 0.554 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.510 |
CLV_PCSK_FUR_1 | 169 | 173 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.437 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.576 |
CLV_PCSK_PC1ET2_1 | 387 | 389 | PF00082 | 0.534 |
CLV_PCSK_PC7_1 | 383 | 389 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.688 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.673 |
DEG_SPOP_SBC_1 | 302 | 306 | PF00917 | 0.698 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 219 | 226 | PF00134 | 0.556 |
DOC_MAPK_gen_1 | 292 | 299 | PF00069 | 0.539 |
DOC_MAPK_HePTP_8 | 322 | 338 | PF00069 | 0.670 |
DOC_MAPK_HePTP_8 | 61 | 73 | PF00069 | 0.542 |
DOC_MAPK_MEF2A_6 | 41 | 48 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 64 | 73 | PF00069 | 0.548 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.639 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.458 |
DOC_PP2B_PxIxI_1 | 16 | 22 | PF00149 | 0.606 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.658 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.820 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.702 |
LIG_14-3-3_CanoR_1 | 130 | 138 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 169 | 175 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 235 | 241 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 64 | 68 | PF00244 | 0.597 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.546 |
LIG_eIF4E_1 | 402 | 408 | PF01652 | 0.659 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.760 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.676 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.659 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.707 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.508 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.596 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.631 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.596 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.673 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.632 |
LIG_SH2_GRB2like | 402 | 405 | PF00017 | 0.495 |
LIG_SH2_SRC | 137 | 140 | PF00017 | 0.396 |
LIG_SH2_SRC | 402 | 405 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 120 | 124 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.453 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.639 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.712 |
LIG_SUMO_SIM_anti_2 | 277 | 283 | PF11976 | 0.497 |
LIG_SUMO_SIM_anti_2 | 333 | 338 | PF11976 | 0.600 |
LIG_SUMO_SIM_par_1 | 17 | 22 | PF11976 | 0.655 |
LIG_SUMO_SIM_par_1 | 277 | 283 | PF11976 | 0.608 |
LIG_SxIP_EBH_1 | 23 | 33 | PF03271 | 0.540 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.527 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.596 |
LIG_WW_3 | 27 | 31 | PF00397 | 0.592 |
MOD_CDK_SPK_2 | 245 | 250 | PF00069 | 0.495 |
MOD_CDK_SPK_2 | 442 | 447 | PF00069 | 0.700 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.762 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.632 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.662 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.651 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.678 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.600 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.731 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.686 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.597 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.758 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.559 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.527 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.524 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.681 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.659 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.537 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.691 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.481 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.745 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.723 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.725 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.693 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.714 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.763 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.533 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.638 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.715 |
MOD_NEK2_2 | 63 | 68 | PF00069 | 0.540 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.607 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.538 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.670 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.589 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.646 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.542 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.589 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.651 |
MOD_Plk_2-3 | 374 | 380 | PF00069 | 0.586 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.672 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.617 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.583 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.646 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.606 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.821 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.700 |
MOD_SUMO_rev_2 | 205 | 215 | PF00179 | 0.528 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 459 | 461 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.503 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY58 | Leptomonas seymouri | 46% | 85% |
A0A422MPI6 | Trypanosoma rangeli | 24% | 100% |
A4HBJ3 | Leishmania braziliensis | 65% | 100% |
A4I9T3 | Leishmania infantum | 99% | 100% |
C9ZMU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9B4U4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q382 | Leishmania major | 89% | 100% |