| 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: 7 |
| NetGPI | no | yes: 0, no: 7 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IC04
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006470 | protein dephosphorylation | 5 | 8 |
| GO:0006793 | phosphorus metabolic process | 3 | 8 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
| GO:0008152 | metabolic process | 1 | 8 |
| GO:0009987 | cellular process | 1 | 8 |
| GO:0016311 | dephosphorylation | 5 | 8 |
| GO:0019538 | protein metabolic process | 3 | 8 |
| GO:0036211 | protein modification process | 4 | 8 |
| GO:0043170 | macromolecule metabolic process | 3 | 8 |
| GO:0043412 | macromolecule modification | 4 | 8 |
| GO:0044237 | cellular metabolic process | 2 | 8 |
| GO:0044238 | primary metabolic process | 2 | 8 |
| GO:0071704 | organic substance metabolic process | 2 | 8 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
| GO:0009966 | regulation of signal transduction | 4 | 1 |
| GO:0009968 | negative regulation of signal transduction | 5 | 1 |
| GO:0010646 | regulation of cell communication | 4 | 1 |
| GO:0010648 | negative regulation of cell communication | 5 | 1 |
| GO:0023051 | regulation of signaling | 3 | 1 |
| GO:0023057 | negative regulation of signaling | 4 | 1 |
| GO:0043408 | regulation of MAPK cascade | 6 | 1 |
| GO:0043409 | negative regulation of MAPK cascade | 7 | 1 |
| GO:0048519 | negative regulation of biological process | 3 | 1 |
| GO:0048523 | negative regulation of cellular process | 4 | 1 |
| GO:0048583 | regulation of response to stimulus | 3 | 1 |
| GO:0048585 | negative regulation of response to stimulus | 4 | 1 |
| GO:0050789 | regulation of biological process | 2 | 1 |
| GO:0050794 | regulation of cellular process | 3 | 1 |
| GO:0065007 | biological regulation | 1 | 1 |
| GO:1902531 | regulation of intracellular signal transduction | 5 | 1 |
| GO:1902532 | negative regulation of intracellular signal transduction | 6 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 8 |
| GO:0004721 | phosphoprotein phosphatase activity | 3 | 8 |
| GO:0008138 | protein tyrosine/serine/threonine phosphatase activity | 4 | 8 |
| GO:0016787 | hydrolase activity | 2 | 8 |
| GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 8 |
| GO:0016791 | phosphatase activity | 5 | 8 |
| GO:0042578 | phosphoric ester hydrolase activity | 4 | 8 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 117 | 121 | PF00656 | 0.715 |
| CLV_C14_Caspase3-7 | 193 | 197 | PF00656 | 0.510 |
| CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.352 |
| CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.705 |
| CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.705 |
| CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.593 |
| CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.699 |
| DEG_APCC_DBOX_1 | 316 | 324 | PF00400 | 0.421 |
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.684 |
| DEG_SCF_FBW7_1 | 174 | 181 | PF00400 | 0.602 |
| DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.795 |
| DOC_CKS1_1 | 153 | 158 | PF01111 | 0.696 |
| DOC_CKS1_1 | 165 | 170 | PF01111 | 0.614 |
| DOC_CKS1_1 | 175 | 180 | PF01111 | 0.511 |
| DOC_CYCLIN_yCln2_LP_2 | 77 | 83 | PF00134 | 0.590 |
| DOC_MAPK_DCC_7 | 88 | 98 | PF00069 | 0.584 |
| DOC_MAPK_gen_1 | 327 | 337 | PF00069 | 0.410 |
| DOC_MAPK_gen_1 | 88 | 96 | PF00069 | 0.688 |
| DOC_MAPK_MEF2A_6 | 89 | 98 | PF00069 | 0.760 |
| DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.696 |
| DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.607 |
| DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.586 |
| DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.705 |
| DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.715 |
| DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.698 |
| DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.620 |
| DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.517 |
| DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.694 |
| DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.684 |
| DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.665 |
| LIG_14-3-3_CanoR_1 | 128 | 136 | PF00244 | 0.718 |
| LIG_14-3-3_CanoR_1 | 188 | 192 | PF00244 | 0.503 |
| LIG_14-3-3_CanoR_1 | 317 | 321 | PF00244 | 0.473 |
| LIG_APCC_ABBA_1 | 272 | 277 | PF00400 | 0.430 |
| LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.705 |
| LIG_FHA_1 | 153 | 159 | PF00498 | 0.727 |
| LIG_FHA_1 | 175 | 181 | PF00498 | 0.657 |
| LIG_FHA_1 | 209 | 215 | PF00498 | 0.483 |
| LIG_FHA_2 | 115 | 121 | PF00498 | 0.714 |
| LIG_FHA_2 | 187 | 193 | PF00498 | 0.508 |
| LIG_FHA_2 | 210 | 216 | PF00498 | 0.371 |
| LIG_FHA_2 | 248 | 254 | PF00498 | 0.397 |
| LIG_FHA_2 | 285 | 291 | PF00498 | 0.501 |
| LIG_FHA_2 | 37 | 43 | PF00498 | 0.728 |
| LIG_FHA_2 | 71 | 77 | PF00498 | 0.793 |
| LIG_Integrin_isoDGR_2 | 332 | 334 | PF01839 | 0.430 |
| LIG_LIR_Apic_2 | 124 | 130 | PF02991 | 0.721 |
| LIG_LIR_Gen_1 | 268 | 278 | PF02991 | 0.382 |
| LIG_LIR_Nem_3 | 268 | 274 | PF02991 | 0.378 |
| LIG_LIR_Nem_3 | 277 | 281 | PF02991 | 0.372 |
| LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.786 |
| LIG_PTB_Apo_2 | 213 | 220 | PF02174 | 0.471 |
| LIG_PTB_Apo_2 | 337 | 344 | PF02174 | 0.376 |
| LIG_PTB_Phospho_1 | 213 | 219 | PF10480 | 0.515 |
| LIG_RPA_C_Fungi | 300 | 312 | PF08784 | 0.501 |
| LIG_SH2_NCK_1 | 163 | 167 | PF00017 | 0.684 |
| LIG_SH2_STAP1 | 278 | 282 | PF00017 | 0.376 |
| LIG_SH2_STAT3 | 176 | 179 | PF00017 | 0.622 |
| LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.594 |
| LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.436 |
| LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.410 |
| LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.397 |
| LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.480 |
| LIG_SH3_2 | 84 | 89 | PF14604 | 0.737 |
| LIG_SH3_3 | 123 | 129 | PF00018 | 0.665 |
| LIG_SH3_3 | 162 | 168 | PF00018 | 0.710 |
| LIG_SH3_3 | 64 | 70 | PF00018 | 0.761 |
| LIG_SH3_3 | 72 | 78 | PF00018 | 0.727 |
| LIG_SH3_3 | 81 | 87 | PF00018 | 0.691 |
| LIG_TRAF2_1 | 61 | 64 | PF00917 | 0.807 |
| MOD_CDC14_SPxK_1 | 79 | 82 | PF00782 | 0.756 |
| MOD_CDC14_SPxK_1 | 86 | 89 | PF00782 | 0.674 |
| MOD_CDK_SPK_2 | 83 | 88 | PF00069 | 0.735 |
| MOD_CDK_SPxK_1 | 122 | 128 | PF00069 | 0.735 |
| MOD_CDK_SPxK_1 | 76 | 82 | PF00069 | 0.734 |
| MOD_CDK_SPxK_1 | 83 | 89 | PF00069 | 0.715 |
| MOD_CK1_1 | 190 | 196 | PF00069 | 0.544 |
| MOD_CK1_1 | 197 | 203 | PF00069 | 0.412 |
| MOD_CK1_1 | 209 | 215 | PF00069 | 0.560 |
| MOD_CK1_1 | 265 | 271 | PF00069 | 0.501 |
| MOD_CK1_1 | 59 | 65 | PF00069 | 0.746 |
| MOD_CK2_1 | 247 | 253 | PF00069 | 0.430 |
| MOD_CK2_1 | 284 | 290 | PF00069 | 0.501 |
| MOD_CK2_1 | 36 | 42 | PF00069 | 0.725 |
| MOD_CK2_1 | 70 | 76 | PF00069 | 0.786 |
| MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.707 |
| MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.671 |
| MOD_GSK3_1 | 116 | 123 | PF00069 | 0.645 |
| MOD_GSK3_1 | 130 | 137 | PF00069 | 0.584 |
| MOD_GSK3_1 | 174 | 181 | PF00069 | 0.628 |
| MOD_GSK3_1 | 186 | 193 | PF00069 | 0.570 |
| MOD_GSK3_1 | 43 | 50 | PF00069 | 0.704 |
| MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.376 |
| MOD_N-GLC_2 | 242 | 244 | PF02516 | 0.430 |
| MOD_NEK2_1 | 104 | 109 | PF00069 | 0.767 |
| MOD_NEK2_1 | 18 | 23 | PF00069 | 0.675 |
| MOD_NEK2_1 | 284 | 289 | PF00069 | 0.501 |
| MOD_NEK2_1 | 41 | 46 | PF00069 | 0.727 |
| MOD_NEK2_1 | 56 | 61 | PF00069 | 0.730 |
| MOD_NEK2_2 | 43 | 48 | PF00069 | 0.672 |
| MOD_PIKK_1 | 223 | 229 | PF00454 | 0.509 |
| MOD_PIKK_1 | 54 | 60 | PF00454 | 0.738 |
| MOD_PKA_2 | 187 | 193 | PF00069 | 0.508 |
| MOD_PKA_2 | 316 | 322 | PF00069 | 0.421 |
| MOD_PKA_2 | 47 | 53 | PF00069 | 0.707 |
| MOD_PKA_2 | 54 | 60 | PF00069 | 0.727 |
| MOD_PKA_2 | 65 | 71 | PF00069 | 0.744 |
| MOD_Plk_1 | 303 | 309 | PF00069 | 0.376 |
| MOD_Plk_1 | 36 | 42 | PF00069 | 0.748 |
| MOD_Plk_4 | 209 | 215 | PF00069 | 0.464 |
| MOD_Plk_4 | 284 | 290 | PF00069 | 0.501 |
| MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.716 |
| MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.696 |
| MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.616 |
| MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.506 |
| MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.695 |
| MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.686 |
| MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.666 |
| TRG_DiLeu_BaEn_4 | 269 | 275 | PF01217 | 0.501 |
| TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.376 |
| TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.376 |
| TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.430 |
| TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.701 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PES2 | Leptomonas seymouri | 57% | 100% |
| A0A0S4JQR8 | Bodo saltans | 30% | 100% |
| A0A3Q8IJV8 | Leishmania donovani | 100% | 100% |
| A4HND2 | Leishmania braziliensis | 78% | 100% |
| E9AFU2 | Leishmania major | 92% | 100% |
| E9B6Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |