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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B561
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 138 | 142 | PF00656 | 0.728 |
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.840 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.764 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.837 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.764 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.843 |
CLV_PCSK_PC7_1 | 378 | 384 | PF00082 | 0.553 |
CLV_PCSK_PC7_1 | 92 | 98 | PF00082 | 0.835 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.698 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.589 |
DOC_CYCLIN_RxL_1 | 356 | 366 | PF00134 | 0.463 |
DOC_MAPK_gen_1 | 400 | 410 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 415 | 425 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 298 | 305 | PF00069 | 0.493 |
DOC_PP1_SILK_1 | 387 | 392 | PF00149 | 0.519 |
DOC_SPAK_OSR1_1 | 314 | 318 | PF12202 | 0.399 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.794 |
DOC_USP7_MATH_2 | 167 | 173 | PF00917 | 0.544 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.715 |
LIG_14-3-3_CanoR_1 | 153 | 159 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 186 | 194 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 249 | 259 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 351 | 359 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 381 | 386 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 51 | 55 | PF00244 | 0.672 |
LIG_Actin_WH2_2 | 289 | 306 | PF00022 | 0.583 |
LIG_BIR_III_2 | 196 | 200 | PF00653 | 0.812 |
LIG_BIR_III_4 | 238 | 242 | PF00653 | 0.547 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.680 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.574 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.638 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.584 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.414 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.407 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.737 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.654 |
LIG_HCF-1_HBM_1 | 376 | 379 | PF13415 | 0.521 |
LIG_Integrin_RGD_1 | 14 | 16 | PF01839 | 0.544 |
LIG_LIR_Apic_2 | 172 | 177 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.633 |
LIG_MYND_1 | 257 | 261 | PF01753 | 0.615 |
LIG_Pex14_2 | 316 | 320 | PF04695 | 0.455 |
LIG_Pex14_2 | 406 | 410 | PF04695 | 0.436 |
LIG_REV1ctd_RIR_1 | 313 | 323 | PF16727 | 0.473 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.807 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.640 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.628 |
LIG_SH2_STAT3 | 64 | 67 | PF00017 | 0.663 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.704 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.540 |
LIG_SH3_1 | 276 | 282 | PF00018 | 0.639 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.787 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.468 |
LIG_SUMO_SIM_anti_2 | 420 | 428 | PF11976 | 0.576 |
LIG_TRAF2_1 | 147 | 150 | PF00917 | 0.741 |
LIG_WRC_WIRS_1 | 439 | 444 | PF05994 | 0.428 |
MOD_CDC14_SPxK_1 | 183 | 186 | PF00782 | 0.687 |
MOD_CDK_SPxK_1 | 180 | 186 | PF00069 | 0.696 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.840 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.756 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.729 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.527 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.540 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.423 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.723 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.526 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.734 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.540 |
MOD_Cter_Amidation | 93 | 96 | PF01082 | 0.615 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.833 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.736 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.816 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.742 |
MOD_GlcNHglycan | 23 | 27 | PF01048 | 0.699 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.692 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.704 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.660 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.734 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.644 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.716 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.733 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.818 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.600 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.587 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.732 |
MOD_N-GLC_1 | 351 | 356 | PF02516 | 0.387 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.456 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.685 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.513 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.653 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.329 |
MOD_NEK2_2 | 154 | 159 | PF00069 | 0.544 |
MOD_PIKK_1 | 428 | 434 | PF00454 | 0.464 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.479 |
MOD_PKA_1 | 21 | 27 | PF00069 | 0.766 |
MOD_PKA_1 | 381 | 387 | PF00069 | 0.606 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.840 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.588 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.575 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.618 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.764 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.432 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.553 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.540 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.793 |
MOD_PKB_1 | 95 | 103 | PF00069 | 0.837 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.601 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.482 |
MOD_Plk_1 | 428 | 434 | PF00069 | 0.481 |
MOD_Plk_2-3 | 145 | 151 | PF00069 | 0.744 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.565 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.544 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.588 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.456 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.384 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.718 |
MOD_SUMO_rev_2 | 168 | 173 | PF00179 | 0.550 |
MOD_SUMO_rev_2 | 219 | 224 | PF00179 | 0.767 |
MOD_SUMO_rev_2 | 366 | 372 | PF00179 | 0.445 |
TRG_DiLeu_BaLyEn_6 | 247 | 252 | PF01217 | 0.726 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.508 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.699 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.757 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 90 | 93 | PF00400 | 0.766 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.832 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ09 | Leptomonas seymouri | 49% | 92% |
A0A3Q8IIN3 | Leishmania donovani | 83% | 100% |
A4HAY8 | Leishmania braziliensis | 66% | 100% |
A4IA47 | Leishmania infantum | 83% | 100% |