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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H5Q1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.570 |
CLV_PCSK_FUR_1 | 163 | 167 | PF00082 | 0.773 |
CLV_PCSK_FUR_1 | 209 | 213 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.760 |
CLV_PCSK_PC1ET2_1 | 165 | 167 | PF00082 | 0.705 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.746 |
CLV_PCSK_PC1ET2_1 | 285 | 287 | PF00082 | 0.590 |
CLV_PCSK_PC7_1 | 281 | 287 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.528 |
DEG_APCC_DBOX_1 | 292 | 300 | PF00400 | 0.567 |
DEG_SPOP_SBC_1 | 287 | 291 | PF00917 | 0.569 |
DOC_ANK_TNKS_1 | 123 | 130 | PF00023 | 0.581 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.677 |
DOC_USP7_UBL2_3 | 136 | 140 | PF12436 | 0.579 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.821 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.709 |
LIG_14-3-3_CanoR_1 | 176 | 185 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 286 | 296 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 311 | 318 | PF00244 | 0.578 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.802 |
LIG_GBD_Chelix_1 | 22 | 30 | PF00786 | 0.609 |
LIG_HCF-1_HBM_1 | 307 | 310 | PF13415 | 0.493 |
LIG_Integrin_isoDGR_2 | 331 | 333 | PF01839 | 0.532 |
LIG_LIR_Gen_1 | 444 | 453 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.714 |
LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 80 | 84 | PF02991 | 0.657 |
LIG_PDZ_Class_2 | 448 | 453 | PF00595 | 0.529 |
LIG_Pex14_1 | 306 | 310 | PF04695 | 0.523 |
LIG_PTB_Apo_2 | 75 | 82 | PF02174 | 0.531 |
LIG_PTB_Phospho_1 | 75 | 81 | PF10480 | 0.530 |
LIG_SH2_CRK | 355 | 359 | PF00017 | 0.723 |
LIG_SH2_STAT3 | 388 | 391 | PF00017 | 0.585 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.560 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.687 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.665 |
LIG_SUMO_SIM_anti_2 | 65 | 70 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 67 | 72 | PF11976 | 0.627 |
MOD_CDC14_SPxK_1 | 87 | 90 | PF00782 | 0.564 |
MOD_CDK_SPxK_1 | 84 | 90 | PF00069 | 0.748 |
MOD_CDK_SPxxK_3 | 167 | 174 | PF00069 | 0.555 |
MOD_CDK_SPxxK_3 | 84 | 91 | PF00069 | 0.749 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.642 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.565 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.721 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.517 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.770 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.621 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.647 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.520 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.549 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.767 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.685 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.597 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.570 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.710 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.553 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.442 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.604 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.780 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.680 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.731 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.739 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.578 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.721 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.819 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.628 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.649 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.670 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.784 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.710 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.564 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.742 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.703 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.773 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.712 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.706 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.662 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.698 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.621 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.554 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.595 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.755 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.626 |
MOD_N-GLC_1 | 287 | 292 | PF02516 | 0.769 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.668 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.590 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.578 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.515 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.597 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.772 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.672 |
MOD_NEK2_2 | 266 | 271 | PF00069 | 0.674 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.632 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.585 |
MOD_PKA_1 | 91 | 97 | PF00069 | 0.781 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.698 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.629 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.643 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.823 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.495 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.588 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.822 |
MOD_PKB_1 | 90 | 98 | PF00069 | 0.575 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.814 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.619 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.498 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.808 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.597 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.454 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.532 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.553 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.757 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.696 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.699 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.582 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.566 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.741 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.821 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.591 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.801 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.711 |
MOD_SUMO_rev_2 | 19 | 29 | PF00179 | 0.527 |
TRG_DiLeu_BaEn_4 | 438 | 444 | PF01217 | 0.557 |
TRG_DiLeu_BaLyEn_6 | 157 | 162 | PF01217 | 0.603 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.722 |
TRG_ER_diArg_1 | 142 | 145 | PF00400 | 0.687 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 182 | 185 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 90 | 92 | PF00400 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 186 | 190 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 20 | 24 | PF00026 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 212 | 216 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ65 | Leptomonas seymouri | 32% | 76% |
A0A3S7WQN7 | Leishmania donovani | 44% | 88% |
A4HTZ1 | Leishmania infantum | 44% | 88% |
E9AMS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 88% |
Q4QHV4 | Leishmania major | 42% | 100% |