Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4H4Q5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.545 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.481 |
DEG_APCC_DBOX_1 | 37 | 45 | PF00400 | 0.459 |
DEG_APCC_DBOX_1 | 407 | 415 | PF00400 | 0.661 |
DEG_SPOP_SBC_1 | 354 | 358 | PF00917 | 0.561 |
DEG_SPOP_SBC_1 | 377 | 381 | PF00917 | 0.543 |
DOC_CYCLIN_RxL_1 | 1 | 9 | PF00134 | 0.499 |
DOC_CYCLIN_yCln2_LP_2 | 455 | 461 | PF00134 | 0.521 |
DOC_MAPK_gen_1 | 104 | 111 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 104 | 113 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 226 | 234 | PF00069 | 0.450 |
DOC_PP2B_LxvP_1 | 170 | 173 | PF13499 | 0.600 |
DOC_PP2B_LxvP_1 | 196 | 199 | PF13499 | 0.426 |
DOC_PP2B_LxvP_1 | 374 | 377 | PF13499 | 0.686 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.518 |
DOC_USP7_UBL2_3 | 145 | 149 | PF12436 | 0.574 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.811 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 104 | 112 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 30 | 37 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 448 | 458 | PF00244 | 0.673 |
LIG_AP2alpha_2 | 366 | 368 | PF02296 | 0.706 |
LIG_APCC_ABBA_1 | 110 | 115 | PF00400 | 0.582 |
LIG_CaM_IQ_9 | 213 | 228 | PF13499 | 0.554 |
LIG_Clathr_ClatBox_1 | 110 | 114 | PF01394 | 0.467 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.540 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.588 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.581 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.252 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.466 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.536 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.551 |
LIG_LIR_Gen_1 | 150 | 159 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 365 | 376 | PF02991 | 0.707 |
LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.701 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.331 |
LIG_MYND_1 | 258 | 262 | PF01753 | 0.827 |
LIG_NRBOX | 40 | 46 | PF00104 | 0.562 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.342 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.633 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.754 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.456 |
LIG_SH2_NCK_1 | 168 | 172 | PF00017 | 0.531 |
LIG_SH2_NCK_1 | 332 | 336 | PF00017 | 0.754 |
LIG_SH2_NCK_1 | 48 | 52 | PF00017 | 0.490 |
LIG_SH2_PTP2 | 158 | 161 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 48 | 52 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.572 |
LIG_SH2_STAT3 | 308 | 311 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.331 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.526 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.704 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.675 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.717 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.587 |
LIG_SUMO_SIM_anti_2 | 114 | 120 | PF11976 | 0.583 |
LIG_SUMO_SIM_anti_2 | 157 | 163 | PF11976 | 0.526 |
LIG_SUMO_SIM_anti_2 | 9 | 15 | PF11976 | 0.461 |
LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.347 |
LIG_TRAF2_1 | 239 | 242 | PF00917 | 0.393 |
LIG_TYR_ITIM | 220 | 225 | PF00017 | 0.624 |
LIG_WW_3 | 182 | 186 | PF00397 | 0.401 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.583 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.727 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.665 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.782 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.506 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.598 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.638 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.639 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.576 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.725 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.827 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.727 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.785 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.758 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.505 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.516 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.486 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.539 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.421 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.773 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.770 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.623 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.585 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.574 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.592 |
MOD_LATS_1 | 446 | 452 | PF00433 | 0.543 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.783 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.566 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.555 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.559 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.647 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.514 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.507 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.623 |
MOD_PKA_1 | 448 | 454 | PF00069 | 0.544 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.520 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.638 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.510 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.629 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.587 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.486 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.606 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.543 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.553 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.642 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.491 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.595 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.456 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.513 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.760 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.810 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.524 |
MOD_SUMO_rev_2 | 174 | 180 | PF00179 | 0.589 |
MOD_SUMO_rev_2 | 190 | 199 | PF00179 | 0.575 |
MOD_SUMO_rev_2 | 271 | 277 | PF00179 | 0.583 |
TRG_DiLeu_BaEn_1 | 114 | 119 | PF01217 | 0.511 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.476 |
TRG_DiLeu_BaEn_1 | 9 | 14 | PF01217 | 0.453 |
TRG_DiLeu_BaEn_4 | 127 | 133 | PF01217 | 0.373 |
TRG_DiLeu_BaLyEn_6 | 259 | 264 | PF01217 | 0.561 |
TRG_DiLeu_LyEn_5 | 40 | 45 | PF01217 | 0.558 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.632 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.455 |
TRG_ER_diArg_1 | 408 | 411 | PF00400 | 0.661 |
TRG_Pf-PMV_PEXEL_1 | 82 | 86 | PF00026 | 0.566 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKD5 | Leptomonas seymouri | 61% | 100% |
A0A3R7KW02 | Trypanosoma rangeli | 33% | 100% |
A0A3S5H5T3 | Leishmania donovani | 73% | 100% |
A4HSY4 | Leishmania infantum | 73% | 100% |
E9AKX0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4QIY5 | Leishmania major | 73% | 100% |
V5BXU6 | Trypanosoma cruzi | 31% | 100% |